2-propanol has been researched along with Eye Abnormalities in 336 studies
2-Propanol: An isomer of 1-PROPANOL. It is a colorless liquid having disinfectant properties. It is used in the manufacture of acetone and its derivatives and as a solvent. Topically, it is used as an antiseptic.
propan-2-ol : A secondary alcohol that is propane in which one of the hydrogens attached to the central carbon is substituted by a hydroxy group.
Eye Abnormalities: Congenital absence of or defects in structures of the eye; may also be hereditary.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Homozygotes are fully viable and exhibit smaller eye, corneal opacity, adhesion of the iris, cataractous degeneration, and extrusion of the lens nucleus and persistent lens-epithelium attachment." | 3.66 | Dysgenetic lens (dyl)--a new gene in the mouse. ( Hawkins, RK; Sanyal, S, 1979) |
| "The left eye has microphthalmia involving the anterior and posterior segments, microcornea, iris coloboma, chorioretinal dysgenesis, macular dysplasia, absence of retinal vessels, and optic nerve aplasia." | 2.48 | Ophthalmic and systemic findings in interstitial deletions of chromosome 14q: a case report and literature review. ( Aaberg, TM; Droste, PJ; Hassan, AS; Pearce, ZD, 2012) |
| "The echocardiogram revealed an atrial septal defect with interatrial aneurysm." | 2.41 | Atrial septal defect with interatrial aneurysm and Axenfeld-Rieger syndrome. ( Bekir, NA; Güngör, K, 2000) |
| "Axenfeld-Rieger syndrome is a term that can be used to describe a variety of overlapping phenotypes." | 2.41 | Axenfeld-Rieger syndrome in the age of molecular genetics. ( Alward, WL, 2000) |
| "In "idiopathic" forms of pituitary dwarfism, defects limited to either the hypothalamus or pituitary have been suggested by releasing hormone stimulation studies and it is quite likely that specific defects of the hypothalamus, and pituitary, as well as defects in releasing hormonal synthesis and secretion and growth hormone synthesis and secretion all exist." | 2.35 | Hereditary forms of growth hormone deficiency and resistance. ( Rimoin, DL, 1976) |
| "In January 2021, we found one case of Axenfeld-Rieger syndrome combined with pigment dispersion syndrome (PDS), and this patient additionally manifested a symptom of ectropion uveae." | 1.91 | Axenfeld-Rieger syndrome combined with ectropion uveae and pigment dispersion syndrome: A case report. ( Bi, H; Li, Y; Liu, J; Ma, X; Tian, Q; Zhao, Y, 2023) |
| "Syndromic microphthalmia 15 (MCOPS15) is characterized by microphthalmia, coloboma, and developmental delay." | 1.72 | Microcornea, iris and choroidal coloboma, and global developmental delay caused by TENM3 pathogenic variants in a Chinese patient. ( Gu, W; Huang, Y; Xu, K; Zhou, Y, 2022) |
| "Congenital iris cysts are a rare condition in infants that can lead to multiple complications." | 1.62 | Complications of a congenital iris cyst in a newborn. ( Nelson, C; Pierce, B, 2021) |
| "Intraocular pressure was 8 and 26 mm Hg in the right eye and left eye, respectively." | 1.42 | Newborn Glaucoma with Imperforate Pupil. ( Krishnamurthy, R; Mandal, AK; Ramappa, M, 2015) |
| "Klinefelter syndrome is caused by the presence of one or more additional X chromosomes in an affected male." | 1.38 | Ocular anomalies in an infant with Klinefelter Syndrome. ( Juhn, AT; Levin, AV; Nabi, NU, 2012) |
| "Lens coloboma is a rare congenital disorder of crystalline lens characterized by notching of the equator of the lens." | 1.37 | Lens coloboma and associated ocular malformations. ( Hu, Z; Li, J; Ma, X, 2011) |
| "Axenfeld-Rieger syndrome is an ocular anterior segment dysgenesis, autosomal dominantly inherited, commonly associated with glaucoma and systemic anomalies." | 1.34 | [Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome]. ( Kamińska, A; Pawluczyk-Dyjecińska, M; Sokołowska-Oracz, A; Szaflik, JP, 2007) |
| "ARM-associated glaucoma is a bilateral anterior segment dysgenesis disease that affects males and females equally." | 1.34 | Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations. ( Dinu, I; Strungaru, MH; Walter, MA, 2007) |
| "Gillespie syndrome is a rare variant form of aniridia, characterized by mental retardation, nonprogressive cerebellar ataxia, and iris hypoplasia." | 1.33 | Ocular findings in Gillespie-like syndrome: association with a new PAX6 mutation. ( Egel, RT; Hilchie-Schmidt, C; Howarth, RJ; Robinson, D; Ticho, BH; Traboulsi, EI, 2006) |
| "Fuchs' endothelial dystrophy was found in 19 patients." | 1.33 | A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy. ( Baumer, A; Gloor, BP; Kniestedt, C; Stuermer, J; Taralczak, M; Thiel, MA, 2006) |
| " Conversely, selective inactivation of a single Pax6 allele in the distal optic cup revealed primarily cell-autonomous dosage requirements for proper iris differentiation, with no affects on either lens or corneal morphology." | 1.33 | Genetic dissection of Pax6 dosage requirements in the developing mouse eye. ( Ashery-Padan, R; Davis-Silberman, N; Kalich, T; Kroeber, M; Marquardt, T; Oron-Karni, V; Tamm, ER, 2005) |
| "All 3 children also had large aorticopulmonary septal defects which were surgically repaired." | 1.33 | Iris hypoplasia and aorticopulmonary septal defect: a neurocristopathy. ( Bergstrom, CS; Hutchinson, AK; Lambert, SR; Saunders, RA, 2005) |
| " The altered corneal thickness attributable to increased forkhead gene dosage is particularly important, because it may affect the clinical management of certain glaucoma subtypes and lead to excessive treatment." | 1.32 | Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of function. ( Bell, R; Bhattacharya, SS; Blixt, A; Brice, G; Carlsson, P; Hitchings, RA; Johansson, B; John, SW; Jordan, T; Khaw, PT; Lehmann, OJ; Smith, R; Tuft, S, 2003) |
| "Rieger syndrome is a rare, autosomal dominant disorder due to developmental arrest of tissues derived from neural crest ectoderm in the third trimester." | 1.32 | The Rieger syndrome: orofacial manifestations. Case report of a rare condition. ( Lehl, G; Pannu, K; Singh, J, 2003) |
| " In the current study, the possible role of altered PITX2 gene dosage in the etiology of AR was investigated." | 1.32 | Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations. ( Allingham, RR; Damji, KF; Héon, E; Kozlowski, K; Kulak, SC; Levin, AV; Lines, MA; Newlin, A; Ritch, R; Shields, MB; Walter, MA, 2004) |
| "Rieger syndrome is a dysembryogenetic disease in which labyrinthic damage can be associated with other genetic anomalies." | 1.32 | Rieger syndrome: case report. ( Megighian, D; Poli, P; Savastano, M, 2003) |
| "Axenfeld-Rieger Syndrome is a disorder of morphogenesis which is autosomal dominantly inherited." | 1.32 | Posterior embryotoxon may not be a forme fruste of Axenfeld-Rieger's Syndrome. ( Karri, B; Kaye, SB; Sim, KT, 2004) |
| "Intraocular pressure was lowered, and visual field loss was stabilized with topical medications." | 1.31 | Unilateral glaucoma in Sotos syndrome (cerebral gigantism). ( Flynn, JT; Gedde, SJ; Yen, MT, 2000) |
| "We report five cases of complex microphthalmia with other ocular malformations in infants or children, which were evaluated to investigate the relationship between the corneal diameters and total axial length." | 1.31 | Five cases of microphthalmia with other ocular malformations. ( Choi, HY; Kim, HJ; Lee, JE; Lee, JS; Oum, BS; Shin, YG, 2001) |
| "Axenfeld-Rieger syndrome is a genetically heterogeneous, autosomal dominant disorder that is characterized by anterior segment defects, glaucoma, and extraocular anomalies." | 1.31 | Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from Brazil. ( Alward, WL; Betinjane, AJ; Borges, AS; Carani, JC; Nishimura, DY; Sheffield, VC; Stone, EM; Susanna, R, 2002) |
| " The data presented provide additional evidence for the pathogenicity of altered gene dosage of FOXC1 and suggest that a common mechanism is responsible for rearrangements of 6p25." | 1.31 | Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions. ( Bhattacharya, SS; Ebenezer, ND; Ekong, R; Fraser, S; Hitchings, RA; Jordan, T; Khaw, PT; Lehmann, OJ; McGill, JI; Mungall, AJ; Ocaka, L; Povey, S; Sowden, JC; Walter, MA, 2002) |
| "A 17-year-old female with Goltz's syndrome was examined because of visual acuity loss in her right eye." | 1.30 | Focal dermal hypoplasia (Goltz's syndrome). ( Erden, I; Günalp, I; Gündüz, K, 1997) |
| "Patients with Menkes disease may have aberrant lashes, anterior stromal hypoplasia, and retinal degeneration." | 1.30 | Menkes disease. New ocular and electroretinographic findings. ( Bateman, JB; Ferreira, RC; Heckenlively, JR; Menkes, JH, 1998) |
| "Alagille syndrome is associated with a characteristic group of ocular findings without apparent serious functional significance and probably unrelated to fat-soluble vitamin deficiency." | 1.30 | Ocular abnormalities in Alagille syndrome. ( Aclimandos, WA; Baker, AJ; Bentley, C; Bird, AC; Davies, A; Hingorani, M; Mieli-Vergani, G; Nischal, KK; Vivian, A, 1999) |
| "The Alagille syndrome (arteriohepatic dysplasia) is a well-recognized multiple malformation syndrome consisting of a paucity of intrahepatic bile bile ducts, peripheral pulmonary artery hypoplasia with variable cardiac abnormalities, cholestatic facies, butterfly-like vertebral arch defects, and variable ocular anomalies, most commonly posterior embryotoxon and pigmentary retinopathy." | 1.29 | Ocular anomalies in the alagille syndrome (arteriohepatic dysplasia). ( Brodsky, MC; Cunniff, C, 1993) |
| "The first child had a large basal encephalocele, agenesis of the corpus callosum, mild optic atrophy in one eye, a retinal pigment epithelial defect in the other eye and bitemporal hemianopia; the second child had septo-optic dysplasia and the third child had Rieger's anomaly." | 1.26 | Ocular defects and short stature. ( Guyda, HJ; Little, JM; Polomeno, RC; Staudenmaier, C, 1980) |
| "Congenital nonprogressive facial hemiatrophy is reported in association with anisometropia and ipsilateral cornea, iris, angle abnormalities, and juvenile glaucoma." | 1.26 | Congenital nonprogressive facial hemiatrophy with ipsilateral eye abnormalities and juvenile glaucoma. ( Cohen, JS, 1979) |
| "Medical treatment of the glaucoma was successful." | 1.26 | Rieger's anomaly with congenital glaucoma a case presentation of postnatal anterior segment maturation. ( Leib, ML; Little, JM; Saheb, NN, 1979) |
| "The glaucoma was controlled with miotic therapy following an iridectomy." | 1.26 | Russell-Silver dwarfism. ( Howard, RO; Kass, MA; Silverman, JP, 1976) |
| "The Rieger syndrome is characterized by mesoectodermal dysplasia of the iris and cornea, dental defects, in some cases short stature, abnormal external ears, hypertelorism, arachnodactyly, polydactyly, scoliosis, kyphosis, imperforate anus, umbilical hernia, myopathy and in a few cases mental retardation." | 1.25 | Mesoectodermal dysplasia of the iris and cornea, mental retardation and myopathy: a sporadic case. ( Duenas, D; Hiatt, RL; Johnson, WW; Summitt, RL, 1971) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 173 (51.49) | 18.7374 |
| 1990's | 25 (7.44) | 18.2507 |
| 2000's | 68 (20.24) | 29.6817 |
| 2010's | 50 (14.88) | 24.3611 |
| 2020's | 20 (5.95) | 2.80 |
| Authors | Studies |
|---|---|
| Mohan, S | 2 |
| Yang, JF | 1 |
| Roohipourmoallai, R | 1 |
| Straughn, PE | 1 |
| Sherwood, MB | 1 |
| Agarwal-Sinha, S | 1 |
| Zori, RT | 1 |
| Iyer, SSR | 1 |
| Jacobson, A | 1 |
| Bohnsack, BL | 1 |
| Zhou, Y | 1 |
| Xu, K | 1 |
| Gu, W | 1 |
| Huang, Y | 1 |
| Courdier, C | 1 |
| Gemahling, A | 1 |
| Guindolet, D | 1 |
| Barjol, A | 1 |
| Scaramouche, C | 1 |
| Bouneau, L | 1 |
| Calvas, P | 2 |
| Martin, G | 1 |
| Chassaing, N | 1 |
| Plaisancié, J | 1 |
| Agarwal, A | 1 |
| Narang, P | 1 |
| Narang, R | 1 |
| Sheng, Q | 1 |
| Zhai, R | 1 |
| Sun, Y | 1 |
| Fan, X | 1 |
| Ying, Y | 1 |
| Kong, X | 1 |
| Li, Y | 1 |
| Liu, J | 1 |
| Tian, Q | 1 |
| Ma, X | 2 |
| Zhao, Y | 1 |
| Bi, H | 1 |
| Yuan, Y | 1 |
| Wang, W | 1 |
| Xiong, R | 1 |
| Zhang, J | 1 |
| Li, C | 1 |
| Yang, S | 1 |
| Friedman, DS | 1 |
| Foster, PJ | 1 |
| He, M | 1 |
| Lima, FL | 1 |
| Cronemberger, S | 1 |
| Albuquerque, ALB | 1 |
| Barbosa, LF | 1 |
| Cunha, FR | 1 |
| Veloso, AW | 1 |
| Diniz-Filho, A | 1 |
| Friedman, E | 1 |
| De Marco, L | 1 |
| Mansoori, T | 1 |
| Barioulet, L | 1 |
| Tolou, C | 1 |
| Bové, M | 1 |
| Lajoie, J | 1 |
| Maceri, C | 1 |
| Gualino, O | 1 |
| Gualino, V | 1 |
| Chang, M | 1 |
| Ancona-Lezama, D | 1 |
| Shields, CL | 1 |
| Choy, BNK | 1 |
| Zhu, MM | 1 |
| Chan, JCH | 1 |
| Boese, EA | 1 |
| Critser, DB | 1 |
| Fingert, JH | 1 |
| Gupta, S | 1 |
| Sethi, HS | 1 |
| Naik, M | 1 |
| Quiroz Quiroga, MJ | 1 |
| Del Prado, C | 1 |
| Morales, M | 1 |
| Kumar Bafna, R | 1 |
| Tripathi, M | 1 |
| Kumari, S | 1 |
| Ibrahime Asif, M | 1 |
| Lata, S | 1 |
| Kalra, N | 1 |
| Sharma, N | 2 |
| Rohrbach, JM | 1 |
| Arestova, NN | 1 |
| Kalinichenko, RV | 1 |
| Egiyan, NS | 1 |
| Kruglova, TB | 1 |
| Nelson, C | 1 |
| Pierce, B | 1 |
| Georgalas, I | 1 |
| Kymionis, GD | 1 |
| Papaconstantinou, D | 1 |
| Paraskevopoulos, T | 1 |
| Solheim, MH | 1 |
| Clermont, AC | 1 |
| Winnay, JN | 1 |
| Hallstensen, E | 1 |
| Molven, A | 1 |
| Njølstad, PR | 1 |
| Rødahl, E | 1 |
| Kahn, CR | 1 |
| Chang, TC | 2 |
| Bauer, M | 1 |
| Puerta, HS | 1 |
| Greenberg, MB | 1 |
| Cavuoto, KM | 2 |
| Abdel-Salam, GMH | 1 |
| Abdel-Hamid, MS | 1 |
| Mehrez, MI | 1 |
| Kamal, AM | 1 |
| Taher, MB | 1 |
| Afifi, HH | 1 |
| Ramasubramanian, S | 1 |
| Majumder, PD | 1 |
| Troumani, Y | 1 |
| Beral, L | 1 |
| David, T | 1 |
| Bouslous, N | 1 |
| Hassaki, K | 1 |
| Hajji, I | 1 |
| Moutaouakil, A | 1 |
| Spierer, O | 1 |
| Suwannaraj, S | 1 |
| McKeown, CA | 1 |
| Bengarai, W | 1 |
| Chokrani, H | 1 |
| Berraho, A | 2 |
| Torrado, LA | 1 |
| Ho, ML | 1 |
| Brodsky, MC | 3 |
| Rahhal-Ortuño, M | 1 |
| Díaz-Llopis, M | 1 |
| Alonso-Muñoz, L | 1 |
| Rahhal, MS | 1 |
| Kadomoto, S | 1 |
| Uji, A | 1 |
| Tsujikawa, A | 1 |
| Liang, TW | 1 |
| Zhang, CY | 1 |
| Bai, DY | 1 |
| Peng, CX | 1 |
| Bai, XQ | 1 |
| Wu, Q | 1 |
| Zhao, JY | 1 |
| Li, L | 1 |
| Kouisbahi, A | 1 |
| Elorch, H | 1 |
| Mouine, S | 1 |
| Amhoud, K | 1 |
| Ibrahimi, F | 1 |
| Oudbib, M | 1 |
| Shakrawal, J | 1 |
| Selvan, H | 2 |
| Sharma, A | 2 |
| Angmo, D | 2 |
| Kim, S | 1 |
| Thomasy, SM | 1 |
| Raghunathan, VK | 1 |
| Teixeira, LBC | 1 |
| Moshiri, A | 1 |
| FitzGerald, P | 1 |
| Murphy, CJ | 1 |
| Madiq, B | 1 |
| Arfaja, A | 1 |
| Charadi, A | 1 |
| Kreit, M | 1 |
| Bentata, R | 1 |
| Chan, H | 1 |
| Coste, V | 1 |
| Delyfer, MN | 1 |
| Chan, G | 1 |
| Korobelnik, JF | 1 |
| Agarwal, R | 1 |
| Nongrem, G | 1 |
| Maharana, PK | 1 |
| Peter, NM | 1 |
| Leyland, M | 1 |
| Mudhar, HS | 1 |
| Lowndes, J | 1 |
| Owen, KR | 1 |
| Stewart, H | 1 |
| Lee, NY | 1 |
| Lee, YE | 1 |
| Mok, J | 1 |
| Kim, M | 1 |
| Park, SH | 1 |
| Espandar, L | 1 |
| Allingham, RR | 2 |
| Afshari, NA | 1 |
| Masket, S | 1 |
| Wilczyński, M | 1 |
| Owidzka, M | 1 |
| Handor, H | 1 |
| Laghmari, M | 1 |
| Hafidi, Z | 1 |
| Daoudi, C | 1 |
| Daoudi, R | 1 |
| Beby, F | 1 |
| Mandal, AK | 3 |
| Ramappa, M | 1 |
| Krishnamurthy, R | 1 |
| Mansour, AM | 1 |
| Hamade, I | 1 |
| Antonios, RS | 1 |
| Shoaib, KK | 1 |
| Rowe, N | 1 |
| Hing, S | 1 |
| Doyle, JJ | 1 |
| Reddy, AK | 1 |
| Rémond, AL | 1 |
| Bodaghi, B | 1 |
| Le Hoang, P | 1 |
| Brockmann, T | 1 |
| Rossel, M | 1 |
| Salchow, DJ | 1 |
| Gokhale, V | 1 |
| Agarkar, S | 1 |
| Hägglund, AC | 1 |
| Jones, I | 1 |
| Carlsson, L | 1 |
| Bredrup, C | 1 |
| Matejas, V | 1 |
| Barrow, M | 1 |
| Bláhová, K | 1 |
| Bockenhauer, D | 1 |
| Fowler, DJ | 1 |
| Gregson, RM | 1 |
| Maruniak-Chudek, I | 1 |
| Medeira, A | 1 |
| Mendonça, EL | 1 |
| Kagan, M | 1 |
| Koenig, J | 1 |
| Krastel, H | 1 |
| Kroes, HY | 1 |
| Saggar, A | 1 |
| Sawyer, T | 1 |
| Schittkowski, M | 1 |
| Swietliński, J | 1 |
| Thompson, D | 1 |
| VanDeVoorde, RG | 1 |
| Wittebol-Post, D | 1 |
| Woodruff, G | 1 |
| Zurowska, A | 1 |
| Hennekam, RC | 1 |
| Zenker, M | 1 |
| Russell-Eggitt, I | 2 |
| PENN, SW | 1 |
| Demidenko, A | 1 |
| Jakobiec, FA | 1 |
| Hanna, E | 1 |
| Walton, DS | 1 |
| Riise, R | 2 |
| D'haene, B | 1 |
| De Baere, E | 1 |
| Grønskov, K | 1 |
| Brøndum-Nielsen, K | 2 |
| Kumar, RS | 1 |
| Tantisevi, V | 1 |
| Wong, MH | 1 |
| Laohapojanart, K | 1 |
| Chansanti, O | 1 |
| Quek, DT | 1 |
| Koh, VT | 1 |
| MohanRam, LS | 1 |
| Lee, KY | 1 |
| Rojanapongpun, P | 1 |
| Aung, T | 1 |
| Kandori, M | 1 |
| Saishin, Y | 1 |
| Kusaka, S | 1 |
| Shimojyo, H | 1 |
| Otori, Y | 1 |
| Tano, Y | 1 |
| SAUER, JJ | 1 |
| WARREN, AG | 1 |
| VAN CANNEYT, J | 1 |
| KLUYSKENS, J | 1 |
| LIJO PAVIA, J | 1 |
| LACHMAN, R | 1 |
| ROCHER, HL | 1 |
| Coppens, G | 1 |
| Zeyen, T | 1 |
| Gulkilik, G | 1 |
| Erdenoz, S | 1 |
| Oba, EM | 1 |
| Andersson, LS | 1 |
| Axelsson, J | 1 |
| Dubielzig, RR | 1 |
| Lindgren, G | 1 |
| Ekesten, B | 1 |
| Li, J | 1 |
| Hu, Z | 1 |
| McKeone, R | 1 |
| Vieira, H | 1 |
| Gregory-Evans, K | 1 |
| Gregory-Evans, CY | 1 |
| Denny, P | 1 |
| Iliff, BW | 1 |
| Riazuddin, SA | 1 |
| Gottsch, JD | 3 |
| Arnalich-Montiel, F | 1 |
| Irigoyen, C | 1 |
| Barrancos, C | 1 |
| Giasin, O | 1 |
| Khan, RS | 1 |
| Khan, K | 1 |
| Juhn, AT | 1 |
| Nabi, NU | 1 |
| Levin, AV | 2 |
| Pearce, ZD | 1 |
| Droste, PJ | 1 |
| Aaberg, TM | 1 |
| Hassan, AS | 1 |
| Kapoor, KG | 1 |
| Baratz, KH | 1 |
| Barkmeier, AJ | 1 |
| Gupta, V | 1 |
| Srivastava, RM | 1 |
| Rao, A | 1 |
| Mittal, M | 1 |
| Fingert, J | 1 |
| Khan, AO | 1 |
| Aldahmesh, MA | 1 |
| Mohamed, JY | 1 |
| Alkuraya, FS | 1 |
| Jun, AS | 2 |
| Broman, KW | 1 |
| Do, DV | 1 |
| Akpek, EK | 2 |
| Stark, WJ | 1 |
| Gasch, AT | 2 |
| Caruso, RC | 1 |
| Kaler, SG | 2 |
| Kaiser-Kupfer, M | 2 |
| Panicker, SG | 2 |
| Sampath, S | 2 |
| Reddy, AB | 2 |
| Ahmed, N | 1 |
| Hasnain, SE | 1 |
| Komatireddy, S | 1 |
| Chakrabarti, S | 1 |
| Balasubramanian, D | 1 |
| Honkanen, RA | 1 |
| Nishimura, DY | 3 |
| Swiderski, RE | 1 |
| Bennett, SR | 1 |
| Hong, S | 1 |
| Kwon, YH | 1 |
| Stone, EM | 3 |
| Sheffield, VC | 3 |
| Alward, WL | 5 |
| Chan, CC | 2 |
| Datiles, M | 1 |
| Kaiser-Kupfer, MI | 1 |
| Kupfer, C | 1 |
| Marneros, AG | 1 |
| Olsen, BR | 1 |
| Lehmann, OJ | 3 |
| Tuft, S | 1 |
| Brice, G | 1 |
| Smith, R | 1 |
| Blixt, A | 1 |
| Bell, R | 1 |
| Johansson, B | 1 |
| Jordan, T | 4 |
| Hitchings, RA | 2 |
| Khaw, PT | 2 |
| John, SW | 2 |
| Carlsson, P | 3 |
| Bhattacharya, SS | 3 |
| Sowden, JC | 2 |
| Erkiliç, K | 1 |
| Ozkiriş, A | 1 |
| Evereklioglu, C | 1 |
| Dogan, H | 1 |
| Hwang, JM | 1 |
| Chung, DC | 1 |
| Traboulsi, EI | 3 |
| Koçak-Midillioglu, I | 1 |
| Karadeniz, N | 1 |
| Yalvaç, I | 1 |
| Koçak-Altintas, AG | 1 |
| Duman, S | 1 |
| ROSSETTI, D | 2 |
| AUVERT, B | 1 |
| LAVAT, J | 1 |
| PAGANI, M | 1 |
| SATO, T | 1 |
| ROI, G | 1 |
| FRANCOIS, J | 10 |
| DE ROUCK, A | 1 |
| WICHMANN, D | 1 |
| COSMETATOS, GF | 1 |
| GREENBERG, R | 1 |
| HAUSTRATE, L | 1 |
| TREVOR-ROPER, PD | 1 |
| CALLAHAN, A | 1 |
| HUERKAMP, B | 1 |
| Schnyder, UW | 1 |
| Landolt, E | 1 |
| Martz, G | 1 |
| MACDIARMID, DC | 2 |
| LEVY, WJ | 2 |
| BURIAN, HM | 1 |
| RICE, MH | 1 |
| ALLEN, L | 2 |
| SCHLOSSMAN, A | 1 |
| HAVENER, WH | 1 |
| LEMMINGSON, W | 2 |
| RIETHE, P | 1 |
| COLLIER, M | 3 |
| GROVE, JH | 1 |
| SHAW, MW | 1 |
| BOURQUE, G | 1 |
| DIGEORGE, AM | 1 |
| OLMSTED, RW | 1 |
| HARLEY, RD | 1 |
| DRENCKHAHN, FO | 1 |
| BEHNKE, H | 1 |
| VEIRS, ER | 2 |
| BROWN, W | 1 |
| APPELMANS, M | 1 |
| MICHIELS, J | 1 |
| VEREECKEN, E | 1 |
| BUSCH, G | 1 |
| WEISKOPF, J | 1 |
| BUSCH, KT | 1 |
| de HAAS, E | 1 |
| HOUTSMULLER, AJ | 1 |
| HIROKAWA, T | 1 |
| MIZUSHIMA, M | 1 |
| MATSUO, H | 1 |
| OUCHI, M | 1 |
| STAFFORD, WR | 1 |
| STUART, JA | 1 |
| FRANDSEN, E | 1 |
| NATH, K | 1 |
| NEMA, HV | 1 |
| SHUKLA, BR | 1 |
| FORSIUS, H | 2 |
| ERIKSSON, A | 1 |
| HENKIND, P | 2 |
| SIGEL, IM | 1 |
| CARR, RE | 1 |
| REED, TE | 1 |
| FALLS, HF | 1 |
| GOUGNARD-RION, C | 1 |
| PARIS, L | 1 |
| NENQUIN-KLAASSEN, E | 1 |
| BRIHAYE-VAN GEER TRUYDEN, M | 1 |
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| FILIU, M | 1 |
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| OGIELSKA, E | 1 |
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| Niederberger, H | 1 |
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| Puri, P | 1 |
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| GUERRA GRANDE, JM | 1 |
| WAGNER, F | 1 |
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| Ritch, R | 4 |
| Shields, MB | 2 |
| Damji, KF | 1 |
| Newlin, A | 1 |
| Walter, MA | 8 |
| Megighian, D | 1 |
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| Lambert, SR | 2 |
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| Dressler, P | 1 |
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| Wissinger, B | 2 |
| Gramer, E | 2 |
| Grieshaber, MC | 1 |
| Orgul, S | 1 |
| Bruder, E | 1 |
| Hadziselimovic, F | 1 |
| Flammer, J | 1 |
| Ticho, BH | 1 |
| Hilchie-Schmidt, C | 1 |
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| Howarth, RJ | 1 |
| Robinson, D | 1 |
| Hollander, DA | 2 |
| Sarfarazi, M | 2 |
| Stoilov, I | 2 |
| Wood, IS | 2 |
| Fredrick, DR | 2 |
| Alvarado, JA | 2 |
| Honkanen, R | 1 |
| Cossari, AJ | 1 |
| Strungaru, MH | 1 |
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| Ito, YA | 1 |
| Footz, TK | 1 |
| Courtens, W | 1 |
| Espana, EM | 1 |
| Mora, R | 1 |
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| Loewenstein, A | 1 |
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| Srivastava, SP | 1 |
| Kamińska, A | 1 |
| Sokołowska-Oracz, A | 1 |
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| Little, JM | 2 |
| Hodgson, SV | 1 |
| Saunders, KE | 1 |
| Romanchuk, KG | 1 |
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21 reviews available for 2-propanol and Eye Abnormalities
| Article | Year |
|---|---|
[Treatment of traumatic iris defects].
Topics: Aniridia; Eye Abnormalities; Eye Injuries; Humans; Iris | 2013 |
Ophthalmic and systemic findings in interstitial deletions of chromosome 14q: a case report and literature review.
Topics: Abnormalities, Multiple; Anophthalmos; Chromosome Deletion; Chromosomes, Human, Pair 14; Coloboma; E | 2012 |
Fox's in development and disease.
Topics: Animals; Anterior Eye Segment; Cornea; DNA-Binding Proteins; Eye Abnormalities; Forkhead Transcripti | 2003 |
[Ocular malformations: management].
Topics: Cornea; Eye; Eye Abnormalities; Humans; Iris; Lens, Crystalline; Microphthalmos | 1983 |
Congenital ocular disease in the foal.
Topics: Animals; Animals, Newborn; Cataract; Ciliary Body; Cornea; Ectropion; Entropion; Eye; Eye Abnormalit | 1984 |
Normal and abnormal ocular development in man.
Topics: Chromosome Aberrations; Chromosome Disorders; Coloboma; Corneal Ulcer; Ectoderm; Eye; Eye Abnormalit | 1982 |
Rehabilitation of a child with partial unilateral cryptophthalmos and multiple congenital anomalies.
Topics: Abnormalities, Multiple; Adult; Child, Preschool; Coloboma; Eye Abnormalities; Eyelids; Face; Female | 1995 |
[Williams-Beuren syndrome: diagnosis and ocular manifestations].
Topics: Adult; Eye Abnormalities; Female; Humans; Iris; Retinal Vessels; Williams Syndrome | 1995 |
[Color and form changes in the iris].
Topics: Diagnosis, Differential; Eye Abnormalities; Eye Color; Humans; Iris; Iris Diseases; Iris Neoplasms; | 1999 |
Atrial septal defect with interatrial aneurysm and Axenfeld-Rieger syndrome.
Topics: Abnormalities, Multiple; Adult; Anterior Eye Segment; Echocardiography; Eye Abnormalities; Face; Fem | 2000 |
Axenfeld-Rieger syndrome in the age of molecular genetics.
Topics: Anterior Eye Segment; Chromosomes, Human, Pair 13; Chromosomes, Human, Pair 4; Chromosomes, Human, P | 2000 |
[Rieger syndrome].
Topics: Abnormalities, Multiple; Coloboma; Eye Abnormalities; Humans; Iris; Syndrome | 2001 |
Axenfeld-Rieger and iridocorneal endothelial syndromes: two spectra of disease with striking similarities and differences.
Topics: Cornea; Corneal Diseases; Diagnosis, Differential; Endothelium, Corneal; Eye Abnormalities; Humans; | 2001 |
Congenital ophthalmic anomalies in cattle.
Topics: Albinism; Animals; Anophthalmos; Cataract; Cattle; Cattle Diseases; Coloboma; Exophthalmos; Eye Abno | 1976 |
Hereditary forms of growth hormone deficiency and resistance.
Topics: Abnormalities, Multiple; Africa; Anencephaly; Animals; Brain; Cleft Lip; Cleft Palate; Drug Resistan | 1976 |
[Clinical ocular biometry (oculometry)].
Topics: Accommodation, Ocular; Anterior Chamber; Biometry; Cornea; Corneal Diseases; Eye; Eye Abnormalities; | 1976 |
Selected eye defects of special importance in pediatrics.
Topics: Bibliographies as Topic; Cataract; Child; Child, Preschool; Coloboma; Ectopia Lentis; Eye Abnormalit | 1987 |
Neonatal ophthalmology.
Topics: Animals; Animals, Newborn; Anophthalmos; Blepharitis; Cataract; Chorioretinitis; Coloboma; Conjuncti | 1985 |
[Eye anomalies in chromosomal aberrations].
Topics: Abnormalities, Multiple; Aneuploidy; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Huma | 1971 |
Oral manifestations of systemic genetic disorders. 3.
Topics: Abnormalities, Multiple; Anodontia; Central Nervous System Diseases; Cornea; Ectodermal Dysplasia; E | 1971 |
[Ocular signs of trisomy 13. General review].
Topics: Anterior Chamber; Brain; Cataract; Child; Child, Preschool; Choroid; Chromosome Aberrations; Chromos | 1971 |
1 trial available for 2-propanol and Eye Abnormalities
| Article | Year |
|---|---|
Fourteen-Year Outcome of Angle-Closure Prevention with Laser Iridotomy in the Zhongshan Angle-Closure Prevention Study: Extended Follow-up of a Randomized Controlled Trial.
Topics: Acute Disease; Eye Abnormalities; Follow-Up Studies; Glaucoma; Glaucoma, Angle-Closure; Gonioscopy; | 2023 |
314 other studies available for 2-propanol and Eye Abnormalities
| Article | Year |
|---|---|
Polycoria Due to Extensive Persistent Pupillary Membranes.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases; Pupil Disorders | 2021 |
Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion.
Topics: Cataract; Chromosome Deletion; Eye Abnormalities; Humans; Iris; Male; Microphthalmos; Persistent Hyp | 2021 |
Anterior megalophthalmos in sisters with Witteveen-Kolk syndrome.
Topics: Eye Abnormalities; Eye Diseases, Hereditary; Female; Genetic Diseases, X-Linked; Humans; Hydrophthal | 2022 |
Microcornea, iris and choroidal coloboma, and global developmental delay caused by TENM3 pathogenic variants in a Chinese patient.
Topics: China; Coloboma; Eye Abnormalities; Humans; Infant; Iris; Male; Membrane Proteins; Microphthalmos; N | 2022 |
EPHA2 biallelic disruption causes syndromic complex microphthalmia with iris hypoplasia.
Topics: Aniridia; Cataract; Eye Abnormalities; Eye Proteins; Homeodomain Proteins; Humans; Iris; Microphthal | 2022 |
When the savior becomes a demon: Silicon oil synechia-induced glaucoma.
Topics: Anterior Eye Segment; Eye Abnormalities; Glaucoma; Glaucoma, Angle-Closure; Gonioscopy; Humans; Intr | 2022 |
Iris abnormalities may influence the efficacy and filtration strategies of Posner-Schlossman syndrome: a retrospective study involving trabeculectomy, ExPRESS and Ahmed valve implants.
Topics: Eye Abnormalities; Follow-Up Studies; Glaucoma; Glaucoma Drainage Implants; Glaucoma, Open-Angle; Hu | 2023 |
Axenfeld-Rieger syndrome combined with ectropion uveae and pigment dispersion syndrome: A case report.
Topics: Adult; Corneal Diseases; Ectropion; Eye Abnormalities; Female; Glaucoma; Humans; Iris; Iris Diseases | 2023 |
Traboulsi syndrome without features of Marfan syndrome caused by a novel homozygous
Topics: Adolescent; Consanguinity; Craniofacial Abnormalities; Ectopia Lentis; Eye Abnormalities; Female; Fi | 2023 |
Qualitative ultrasound biomicroscopy in glaucoma.
Topics: Ciliary Body; Eye Abnormalities; Glaucoma; Glaucoma, Angle-Closure; Humans; Iris; Iris Diseases; Mic | 2023 |
[Iris pigment epithelial cyst dislocated into the vitreous].
Topics: Cysts; Eye Abnormalities; Humans; Iris; Iris Diseases | 2023 |
Vascular perfusion in persistent pupillary membrane of the iris.
Topics: Antineoplastic Agents; Eye Abnormalities; Female; Fluorescein Angiography; Humans; Infant; Iris; Ret | 2019 |
Bilateral segmental accessory iris membrane with narrow anterior chamber angle.
Topics: Anterior Chamber; Eye Abnormalities; Humans; Iris; Microscopy, Acoustic; Tomography, Optical Coheren | 2019 |
High Iris Insertion in Axenfeld-Rieger Syndrome.
Topics: Adult; Anterior Eye Segment; Cornea; Eye Abnormalities; Eye Diseases, Hereditary; Gonioscopy; Humans | 2020 |
Temporal iridofundal coloboma with persistent pupillary membranes with persistent fetal vasculature.
Topics: Coloboma; Eye Abnormalities; Humans; Iris; Iris Diseases; Persistent Hyperplastic Primary Vitreous; | 2020 |
A child with bilateral iris cysts: Iris Flocculi.
Topics: Child; Cysts; Eye Abnormalities; Flocculation; Humans; Iris; Iris Diseases; Male; Slit Lamp Microsco | 2020 |
The enigma of subnormal vision in persistent pupillary membrane.
Topics: Eye Abnormalities; Humans; Iris; Membranes; Vision Disorders; Vision, Low | 2021 |
[On the question of the lens coloboma].
Topics: Coloboma; Eye Abnormalities; Humans; Iris; Lens, Crystalline | 2021 |
[Laser corepraxy in mesodermal iris dysgenesis (Axenfeld-Rieger syndrome) (case report)].
Topics: Anterior Eye Segment; Child; Eye Abnormalities; Eye Diseases, Hereditary; Humans; Iris; Lasers | 2021 |
Complications of a congenital iris cyst in a newborn.
Topics: Cysts; Eye Abnormalities; Humans; Infant; Infant, Newborn; Iris; Iris Diseases | 2021 |
Choroidal Coloboma Presenting as Leukocoria.
Topics: Child; Coloboma; Disease Progression; Eye Abnormalities; Greece; Humans; Iris; Iris Diseases; Male; | 2017 |
Iris Malformation and Anterior Segment Dysgenesis in Mice and Humans With a Mutation in PI 3-Kinase.
Topics: Animals; Anterior Eye Segment; Class Ia Phosphatidylinositol 3-Kinase; Disease Models, Animal; DNA; | 2017 |
Ophthalmic findings in Frank-ter Haar syndrome: report of a sibling pair.
Topics: Abnormalities, Multiple; Adaptor Proteins, Signal Transducing; Amblyopia; Child, Preschool; Choroid; | 2017 |
Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation.
Topics: Adult; Cataract; Codon, Nonsense; Coloboma; Consanguinity; Cornea; DNA Mutational Analysis; Ear; Exo | 2018 |
Acorea: A rare congenital anomaly.
Topics: Eye Abnormalities; Humans; Iris; Male; Pupil Disorders; Tomography, Optical Coherence; Vision Disord | 2018 |
[Persistent pupillary membrane].
Topics: Adult; Eye Abnormalities; Female; France; Humans; Iris; Photography; Pupil; Pupil Disorders | 2018 |
[Bilateral "Mickey Mouse" posterior synechiae].
Topics: Adult; Cartoons as Topic; Eye Abnormalities; Female; Humans; Iris; Iris Diseases | 2018 |
Outcome of optical iridectomy in Peters anomaly.
Topics: Anterior Eye Segment; Child, Preschool; Corneal Opacity; Eye Abnormalities; Female; Follow-Up Studie | 2018 |
Axenfeld-Rieger syndrome.
Topics: Abnormalities, Multiple; Anterior Eye Segment; Cataract; Child; Ectropion; Eye Abnormalities; Eye Di | 2018 |
Posterior Embryotoxon, Corectopia, and Cerebellar Dysgenesis.
Topics: Abnormalities, Multiple; Adolescent; Anterior Eye Segment; Cerebellum; Eye Abnormalities; Eye Diseas | 2018 |
An unusual case of acoria in Sturge-Weber syndrome.
Topics: Eye Abnormalities; Female; Glaucoma; Humans; Intraocular Pressure; Iris; Middle Aged; Port-Wine Stai | 2020 |
Anterior Segment Optical Coherence Tomography Angiography in a Patient With Persistent Pupillary Membrane.
Topics: Anterior Eye Segment; Eye Abnormalities; Female; Fluorescein Angiography; Humans; Iris; Middle Aged; | 2018 |
[Clinical characteristics and treatment of congenital fibrovascular pupillary membranes].
Topics: Child; Eye Abnormalities; Female; Humans; Intraocular Pressure; Iris; Male; Pupil; Retrospective Stu | 2018 |
Bilateral persistent pupillary membrane in an adult patient: A case report.
Topics: Adult; Eye Abnormalities; Female; Humans; Iris; Pupil Disorders; Vision Disorders | 2018 |
Double trouble: Microspherophakia with Axenfeld-Rieger anomaly.
Topics: Abnormalities, Multiple; Adolescent; Anterior Chamber; Anterior Eye Segment; Corneal Diseases; Ectop | 2019 |
Ocular phenotypic consequences of a single copy deletion of the
Topics: Adaptor Proteins, Signal Transducing; Animals; Cataract; Cell Cycle Proteins; Corneal Stroma; Descem | 2019 |
The Missing Mesenchyme Captured-Axenfeld-Rieger Anomaly.
Topics: Anterior Eye Segment; Eye Abnormalities; Eye Diseases, Hereditary; Humans; Iris; Mesoderm | 2019 |
[Bilateral iris mammillations: A case report].
Topics: Child, Preschool; Choroid Neoplasms; Corneal Dystrophies, Hereditary; Diagnosis, Differential; Eye A | 2019 |
[Persistent pupillary membrane (Wachendorf membrane)].
Topics: Eye Abnormalities; Humans; Infant, Newborn; Iris; Male; Mydriatics; Pupil; Pupil Disorders | 2019 |
Unilateral acute hydrops in a child with bilateral microcornea and iridofundal coloboma.
Topics: Abnormalities, Multiple; Acute Disease; Adolescent; Anti-Bacterial Agents; Antihypertensive Agents; | 2019 |
PAX6 mutation in association with ptosis, cataract, iris hypoplasia, corneal opacification and diabetes: a new variant of familial aniridia?
Topics: Adolescent; Adult; Aged; Aniridia; Blepharoptosis; Blood Glucose; Corneal Opacity; Diabetes Mellitus | 2013 |
Three cases with unusual ophthalmic phenotypes of congenital aniridia.
Topics: Abnormalities, Multiple; Adult; Aniridia; Anterior Eye Segment; Cornea; Corneal Opacity; Eye Abnorma | 2013 |
Stromal duplication of the iris.
Topics: Eye Abnormalities; Gonioscopy; Humans; Hyperopia; Intraocular Pressure; Iridectomy; Iris; Laser Ther | 2013 |
Cataract surgical problem: February consultation #1.
Topics: Cataract; Cataract Extraction; Coloboma; Cornea; Craniofacial Abnormalities; Eye Abnormalities; Foot | 2014 |
[Iris atrophy in a case of Rieger's anomaly].
Topics: Anterior Eye Segment; Atrophy; Child, Preschool; Eye Abnormalities; Eye Diseases, Hereditary; Humans | 2014 |
Systemic abnormalities in children with congenital optic disc excavations.
Topics: Cataract; Child; Child, Preschool; Coloboma; Corneal Opacity; Eye Abnormalities; Female; Humans; Inf | 2015 |
Newborn Glaucoma with Imperforate Pupil.
Topics: Cornea; Eye Abnormalities; Humans; Hydrophthalmos; Infant; Intraocular Pressure; Iris; Male; Plastic | 2015 |
Sequential argon-YAG laser membranotomy of extensive persistent pupillary membrane with visual loss.
Topics: Adult; Argon; Eye Abnormalities; Female; Humans; Iris; Iris Diseases; Laser Coagulation; Laser Thera | 2015 |
Peeling the Persistent Pupillary Membrane.
Topics: Child; Eye Abnormalities; Female; Humans; Iris; Pupil; Treatment Outcome; Visual Acuity; Vitreoretin | 2016 |
Bilateral Persistent Pupillary Membranes.
Topics: Adult; Eye Abnormalities; Female; Glare; Humans; Iris; Mydriatics; Pupil; Vision Disorders; Visual A | 2016 |
[Congenital iris cyst].
Topics: Adult; Cysts; Eye Abnormalities; Female; Humans; Iris; Iris Diseases | 2016 |
Progressive idiopathic tractional corectopia with iris thinning.
Topics: Eye Abnormalities; Humans; Infant; Iris; Male; Ophthalmologic Surgical Procedures; Pupil Disorders | 2016 |
Persistent Pupillary Membrane.
Topics: Adolescent; Amblyopia; Eye Abnormalities; Humans; Iris; Male | 2017 |
A novel mouse model of anterior segment dysgenesis (ASD): conditional deletion of
Topics: Animals; Animals, Newborn; Anterior Eye Segment; Cell Lineage; Ciliary Body; Disease Models, Animal; | 2017 |
Ophthalmological aspects of Pierson syndrome.
Topics: Abnormalities, Multiple; Eye Abnormalities; Female; Humans; Infant, Newborn; Iris; Laminin; Male; Mu | 2008 |
Intermittent iris bombe.
Topics: Eye Abnormalities; Iris; Iris Diseases | 1948 |
Congenital pupillary-iris-lens membrane with goniodysgenesis: a rare cause of glaucoma and vision loss.
Topics: Anterior Eye Segment; Blindness; Child; Eye Abnormalities; Eye Enucleation; Glaucoma, Neovascular; H | 2009 |
Rieger syndrome is not associated with PAX6 deletion: a correction to Acta Ophthalmol Scand 2001: 79: 201-203.
Topics: Abnormalities, Multiple; Anterior Eye Segment; Eye Abnormalities; Eye Proteins; Face; Gene Deletion; | 2009 |
Plateau iris in Asian subjects with primary angle closure glaucoma.
Topics: Adult; Aged; Aged, 80 and over; Asian People; Ciliary Body; Cross-Sectional Studies; Eye Abnormaliti | 2009 |
Pupilloplasty for congenital pupillary-iris-lens membrane with 25-gauge vitreous cutter.
Topics: Choristoma; Eye Abnormalities; Eye Diseases; Humans; Infant, Newborn; Iris; Lens Diseases; Male; Oph | 2010 |
Anomalies of the iris; report of two cases.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1946 |
Persistent pupillary membrane in the dog.
Topics: Animals; Dogs; Eye; Eye Abnormalities; Fetus; Iris; Pupil | 1946 |
Apparent anophthalmia on one side, microphthalmia with pseudo-coloboma of the iris typical of the other.
Topics: Coloboma; Eye Abnormalities; Humans; Iris | 1945 |
Congenital aniridia (on three observations).
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1945 |
Bilevel complicated bilateral, complicated by bilateral palpebral coloboma and left iris coloboma; total ectromelia of the right upper limb.
Topics: Extremities; Eye Abnormalities; Face; Humans; Iris; Limb Deformities, Congenital | 1945 |
Axenfeld's anomaly.
Topics: Abnormalities, Multiple; Adult; Anterior Eye Segment; Eye Abnormalities; Eye Diseases, Hereditary; F | 2010 |
A case of Joubert syndrome with features of ocular neovascularization.
Topics: Abnormalities, Multiple; Cerebellar Diseases; Cerebellum; Child; Electroretinography; Evoked Potenti | 2010 |
Multiple congenital ocular anomalies in Icelandic horses.
Topics: Animals; Eye Abnormalities; gp100 Melanoma Antigen; Hair Color; Heterozygote; Homozygote; Horse Dise | 2011 |
Lens coloboma and associated ocular malformations.
Topics: Abnormalities, Multiple; Aniridia; Choroid; Coloboma; Eye Abnormalities; Humans; Iris; Lens Subluxat | 2011 |
Foxf2: a novel locus for anterior segment dysgenesis adjacent to the Foxc1 gene.
Topics: Aging; Amino Acid Sequence; Animals; Base Sequence; Biological Specimen Banks; Cornea; DNA; Embryo, | 2011 |
A single-base substitution in the seed region of miR-184 causes EDICT syndrome.
Topics: Cataract; Corneal Dystrophies, Hereditary; Corneal Stroma; Endothelium, Corneal; Eye Abnormalities; | 2012 |
Fixation of subluxated iris-claw anterior chamber intraocular lens in complex case using a retrievable suture technique.
Topics: Adult; Anterior Chamber; Artificial Lens Implant Migration; Eye Abnormalities; Homocystinuria; Human | 2012 |
Corneal thinning phenotypes: an alternative perspective.
Topics: Cataract; Corneal Dystrophies, Hereditary; Eye Abnormalities; Female; Humans; Iris; Male; MicroRNAs; | 2012 |
Ocular anomalies in an infant with Klinefelter Syndrome.
Topics: Cataract; Cataract Extraction; Eye Abnormalities; Humans; Infant; Iris; Klinefelter Syndrome; Male; | 2012 |
Laser photocoagulation of an avulsed persistent pupillary membrane vessel causing recurrent hyphaema.
Topics: Eye Abnormalities; Fluorescein Angiography; Gonioscopy; Humans; Hyphema; Iris; Laser Coagulation; Ma | 2013 |
Clinical correlates to the goniodysgensis among juvenile-onset primary open-angle glaucoma patients.
Topics: Adolescent; Adult; Age of Onset; Anterior Eye Segment; Child; Eye Abnormalities; Family Health; Fema | 2013 |
Congenital glaucoma with acquired peripheral circumferential iris degeneration.
Topics: Antihypertensive Agents; Aryl Hydrocarbon Hydroxylases; Cytochrome P-450 CYP1B1; Drug Therapy, Combi | 2013 |
Endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (edict) syndrome maps to chromosome 15q22.1-q25.3.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anterior Eye Segment; Cataract; Chromosome Mapping; Chro | 2002 |
Menkes' syndrome: ophthalmic findings.
Topics: Abnormalities, Multiple; Adolescent; Child; Child, Preschool; Clinical Trials as Topic; Evoked Poten | 2002 |
Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly.
Topics: Adult; Anterior Eye Segment; Blindness; DNA Mutational Analysis; DNA-Binding Proteins; Eye Abnormali | 2002 |
Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India.
Topics: Adolescent; Adult; Age of Onset; Anterior Eye Segment; Child; Child, Preschool; Cornea; DNA Mutation | 2003 |
A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene.
Topics: Abnormalities, Multiple; Adolescent; Adult; Aged; Anterior Eye Segment; Child; Corneal Opacity; DNA | 2003 |
Congenital iridocorneal malformation in Rieger syndrome.
Topics: Child; Ciliary Body; Cornea; Cryotherapy; Eye Abnormalities; Humans; Intraocular Pressure; Iris; Mal | 2003 |
Age-dependent iris abnormalities in collagen XVIII/endostatin deficient mice with similarities to human pigment dispersion syndrome.
Topics: Aging; Angiogenesis Inhibitors; Animals; Basement Membrane; Ciliary Body; Collagen; Collagen Type XV | 2003 |
Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of function.
Topics: Animals; Anterior Eye Segment; Cornea; DNA-Binding Proteins; Eye Abnormalities; Forkhead Transcripti | 2003 |
Rieger anomaly with bilateral choroidal osteoma: coincidence or association?
Topics: Abnormalities, Multiple; Adolescent; Anterior Eye Segment; Calcinosis; Choroid Neoplasms; Eye Abnorm | 2003 |
A new syndrome of hereditary congenital corneal opacities, cornea guttata, and corectopia.
Topics: Adolescent; Adult; Corneal Opacity; Descemet Membrane; Eye Abnormalities; Eye Diseases, Hereditary; | 2003 |
Eight-year follow-up of Axenfeld-Rieger syndrome with Turner syndrome.
Topics: Abnormalities, Multiple; Adult; Anterior Eye Segment; Eye Abnormalities; Female; Follow-Up Studies; | 2003 |
[Case of mesodermal dysgenesis of the iris and cornea associated with congenital defect of the heart].
Topics: Cardiovascular Abnormalities; Cardiovascular System; Cornea; Eye Abnormalities; Humans; Iris | 1952 |
[Fuchs' heterochromia and puncture of the anterior chamber].
Topics: Anterior Chamber; Cataract; Eye Abnormalities; Humans; Iris; Iris Diseases; Punctures | 1952 |
[Hypotonic action of pilocarpine and eserine in congenital aniridia with glaucoma].
Topics: Aniridia; Eye Abnormalities; Glaucoma; Humans; Iris; Physostigmine; Pilocarpine | 1952 |
A new proposal for the surgical treatment of anterior synechia.
Topics: Cornea; Eye Abnormalities; Humans; Iris; Iris Diseases | 1953 |
[A case of heterochromia iridis with hemisudation of the face].
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases; Pigmentation Disorders; Sweating | 1953 |
[Congenital hereditary aplasia of the iris].
Topics: Eye Abnormalities; Humans; Iris | 1952 |
[New contribution on Fuchs' heterochromia].
Topics: Eye Abnormalities; Humans; Iris | 1952 |
[On the inheritance of iridal fissures and their relation to iridal pigmentation].
Topics: Congenital Abnormalities; Eye Abnormalities; Heredity; Humans; Iris; Iris Diseases; Pigmentation; Tr | 1953 |
[Congenital heterochromia of the iris and its explanation].
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1953 |
Congenital bilateral coloboma of iris and chorioid; a case report.
Topics: Choroid; Coloboma; Congenital Abnormalities; Eye Abnormalities; Humans; Iris; Iris Diseases | 1953 |
[A family showing ocular anomalies of the colobotomous type from unilateral coloboma of the iris to bilateral anophthalmia associated with Bardet-Biedl syndrome].
Topics: Anophthalmos; Bardet-Biedl Syndrome; Coloboma; Eye; Eye Abnormalities; Head; Heredity; Humans; Iris; | 1953 |
[New contribution to the study of Fuchs' heterochromia].
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1954 |
[On a family presenting ocular colobomata ranging from unilateral coloboma of the iris to bilateral anophthalmos associated with Bardet-Biedl syndrome].
Topics: Anophthalmos; Bardet-Biedl Syndrome; Coloboma; Congenital Abnormalities; Eye Abnormalities; Heredity | 1953 |
[Coloboma of the eyeball and a syndrome involving the iris].
Topics: Bone and Bones; Coloboma; Congenital Abnormalities; Eye Abnormalities; Humans; Iris; Syndrome | 1953 |
Iridoschisis.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases; Uveitis, Intermediate | 1954 |
Congenital aniridia.
Topics: Aniridia; Congenital Abnormalities; Eye Abnormalities; Humans; Iris; Iris Diseases | 1955 |
Multiple abnormalities of the iris (mesodermal tissue, atrophy and holes), with secondary glaucoma and deafness; histologic examination of one eye.
Topics: Abnormalities, Multiple; Atrophy; Congenital Abnormalities; Eye Abnormalities; Glaucoma; Hearing Dis | 1956 |
[Causes of unusual appearance of the iris and their relation to iris diagnosis].
Topics: Aging; Congenital Abnormalities; Eye Abnormalities; Humans; Iris; Iris Diseases | 1955 |
[Klippel-Trénaunay syndrome with atypical irien coloboma].
Topics: Angiomatosis; Congenital Abnormalities; Eye Abnormalities; Humans; Iris; Iris Diseases | 1956 |
Aniridia and essential atrophy of the iris.
Topics: Aniridia; Atrophy; Eye Abnormalities; Humans; Iris; Iris Diseases | 1955 |
Aniridia and essential atrophy of the iris.
Topics: Aniridia; Atrophy; Eye Abnormalities; Humans; Iris; Iris Diseases | 1955 |
Aniridia and essential atrophy of the iris.
Topics: Aniridia; Atrophy; Eye Abnormalities; Humans; Iris; Iris Diseases | 1955 |
Aniridia and essential atrophy of the iris.
Topics: Aniridia; Atrophy; Eye Abnormalities; Humans; Iris; Iris Diseases | 1955 |
Congenital iris lesion.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1957 |
Congenital iris lesion.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1957 |
Congenital iris lesion.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1957 |
Congenital iris lesion.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1957 |
External visibility of the region of Schlemm's canal; report on a family with developmental anomalies of cornea, iris, and chamber angle.
Topics: Cornea; Eye Abnormalities; Humans; Iris; Sclera | 1957 |
Congenital anomalies of the iris.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1957 |
Developmental anomalies; a case report on preventable blindness.
Topics: Blindness; Eye Abnormalities; Humans; Iris; Iris Diseases | 1958 |
[Observations on mesodermal dysgenesis of the cornea & iris associated with oligodontia].
Topics: Cornea; Eye Abnormalities; Humans; Iris; Tooth Abnormalities | 1958 |
[Partial circumpupillar aplasia of the left iris with flocculi of the pigmented border].
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1960 |
A family study of aniridia.
Topics: Aniridia; Eye Abnormalities; Humans; Iris; Iris Diseases | 1961 |
Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects.
Topics: Deafness; Eye Abnormalities; Eyelids; Humans; Iris; Lacrimal Apparatus; Waardenburg Syndrome | 1960 |
[Variability in the clinical manifestations of iris defect in 2 families with congenital aniridia].
Topics: Aniridia; Eye Abnormalities; Humans; Iris; Iris Diseases | 1961 |
[Multiple dysplasias in combination with mesodermal dysgenesis of the cornea and iris].
Topics: Congenital Abnormalities; Cornea; Eye Abnormalities; Humans; Iris; Iris Diseases; Medical Records | 1961 |
Congenital moisis associated with a narrow angle of the anterior chamber and abnormally placed iris tissue.
Topics: Anterior Chamber; Eye Abnormalities; Humans; Iris; Iris Diseases; Punishment | 1961 |
[Iridoschisis].
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1959 |
[Dysgenesis mesodermalis et ectodermalis Rieger or Rieger's disease].
Topics: Congenital Abnormalities; Cornea; Eye Abnormalities; Humans; Iris; Iris Diseases | 1960 |
[Circular hypoplasia of the mesodermal iris].
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1959 |
[Left ophthalmic zona. Scleral complications, osteoporosis of the superior maxilla, congenital abnormalities of the iris and fundus of the eye].
Topics: Cornea; Corneal Diseases; Disease; Eye Abnormalities; Herpes Zoster; Humans; Iris; Maxilla; Osteopor | 1959 |
[A patient with Fuch's heterochromia and Recklinghausen's disease].
Topics: Eye Abnormalities; Humans; Iris; Neurofibromatosis 1 | 1962 |
[Gonioscopy in aniridia].
Topics: Aniridia; Eye Abnormalities; Gonioscopy; Humans; Iris; Ophthalmoscopy | 1962 |
Congenital melanosis oculi. Report of a case.
Topics: Eye Abnormalities; Humans; Iris; Melanosis; Sclera | 1962 |
CONGENITAL ANTERIOR STAPHYLOMA.
Topics: Congenital Abnormalities; Cornea; Corneal Diseases; Eye Abnormalities; Humans; Infant; Infant, Newbo | 1963 |
RIEGER'S SYNDROME COMBINED WITH OLIGODONITIA AND FINGER DEFORMITY.
Topics: Anterior Chamber; Anterior Eye Segment; Child; Congenital Abnormalities; Cornea; Eye Abnormalities; | 1963 |
EVOLUTION OF CERTAIN CORNEAL MALFORMATIONS (STUDIES ON A CASE OF MICROCORNEA PLANA CONGENITA WITH ATROPHY OF IRIS AND GLAUCOMA).
Topics: Atrophy; Congenital Abnormalities; Cornea; Corneal Diseases; Eye Abnormalities; Glaucoma; Humans; Ir | 1964 |
EMBRYOTOXON CORNEAE POSTERIUS IN A FAMILY WITH SLIT-PUPIL AND IN CASES WITH OTHER ANOMALIES OF THE IRIS.
Topics: Adolescent; Astigmatism; Cataract; Child; Congenital Abnormalities; Cornea; Eye Abnormalities; Genet | 1964 |
MESODERMAL DYSGENESIS OF THE ANTERIOR SEGMENT: RIEGER'S ANOMALY.
Topics: Anterior Chamber; Anterior Eye Segment; Congenital Abnormalities; Cornea; Eye Abnormalities; Eye Dis | 1965 |
A pedigree of aniridia with a discussion of germinal mosaicism in man.
Topics: Aniridia; Congenital Abnormalities; Eye Abnormalities; Heredity; Humans; Iris; Male; Mosaicism; Pedi | 1955 |
[Heterochromy in Claude Bernard-Horner Syndrome].
Topics: Eye Abnormalities; Horner Syndrome; Humans; Iris; Iris Diseases; Reflex Sympathetic Dystrophy | 1954 |
[Congenital glaucoma associated with a hypoplasia of the iris].
Topics: Eye Abnormalities; Glaucoma; Humans; Iris | 1959 |
[A curious syndrome: deaf-mutism, iridal heterochromia and epilepsy].
Topics: Deafness; Epilepsy; Eye Abnormalities; Humans; Iris; Iris Diseases; Medical Records; Syndrome; Trite | 1959 |
Aniridia with retinal lipid deposits.
Topics: Aniridia; Eye Abnormalities; Iris; Iris Diseases; Lipids; Retina | 1962 |
[A case of developmental abnormalities of the iris--pin hole pupils].
Topics: Eye Abnormalities; Humans; Iris; Pupil; Pupil Disorders | 1962 |
Progression of congenital ectropion uveae.
Topics: Adolescent; Anterior Chamber; Disease Progression; Eye Abnormalities; Glaucoma; Humans; Intraocular | 2003 |
Cobb's tufts: a rare cause of spontaneous hyphaema.
Topics: Blood Vessels; Eye Abnormalities; Fluorescein Angiography; Humans; Hyphema; Iris; Male; Middle Aged | 2001 |
[Typical, bilateral and simultaneous coloboma of the iris, ciliary body, crystalline lens and chorioretina at the entrance of the optic nerve].
Topics: Ciliary Body; Coloboma; Eye Abnormalities; Humans; Iris; Lens, Crystalline; Optic Nerve | 1951 |
[Persistent pupillary membrane].
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases; Pupil Disorders | 1951 |
The Rieger syndrome: orofacial manifestations. Case report of a rare condition.
Topics: Adult; Denture, Partial, Fixed; Eye Abnormalities; Glaucoma; Humans; Iris; Male; Maxilla; Retrognath | 2003 |
Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations.
Topics: Anterior Eye Segment; Chromosome Mapping; Chromosomes, Human, Pair 4; DNA Mutational Analysis; Eye A | 2004 |
Rieger syndrome: case report.
Topics: Adult; Atrophy; Audiometry, Pure-Tone; Auditory Threshold; Brain Stem; Ear, Inner; Eye Abnormalities | 2003 |
Buphthalmos in trisomy 13.
Topics: Abnormalities, Multiple; Chromosomes, Human, Pair 13; Eye Abnormalities; Female; Humans; Infant, New | 2005 |
Familial iridogoniodysgenesis and skeletal anomalies: a probable new autosomal recessive disorder.
Topics: Adult; Bone and Bones; Eye Abnormalities; Facies; Female; Genes, Recessive; Glaucoma; Humans; Iris; | 2004 |
The wing 2 region of the FOXC1 forkhead domain is necessary for normal DNA-binding and transactivation functions.
Topics: Amino Acid Sequence; Animals; Anterior Eye Segment; Child, Preschool; Chlorocebus aethiops; COS Cell | 2004 |
Posterior embryotoxon may not be a forme fruste of Axenfeld-Rieger's Syndrome.
Topics: Abnormalities, Multiple; Adolescent; Anodontia; Eye Abnormalities; Female; Humans; Iris; Maxilla; Sk | 2004 |
PITX2 gain-of-function in Rieger syndrome eye model.
Topics: Alleles; Animals; Blotting, Southern; Chromosome Mapping; Collagen; Cornea; Disease Models, Animal; | 2004 |
Diamond iris retractor configuration for small-pupil extracapsular or intracapsular cataract surgery.
Topics: Cataract; Cataract Extraction; Eye Abnormalities; Humans; Iris; Lens Implantation, Intraocular; Visu | 2004 |
Variable phenotype related to a novel PAX 6 mutation (IVS4+5G>C) in a family presenting congenital nystagmus and foveal hypoplasia.
Topics: Adult; Amino Acid Sequence; Base Sequence; DNA Mutational Analysis; Eye Abnormalities; Eye Proteins; | 2004 |
Iris hypoplasia and aorticopulmonary septal defect: a neurocristopathy.
Topics: Aortopulmonary Septal Defect; Eye Abnormalities; Female; Fetal Diseases; Humans; Infant; Iris; Longi | 2005 |
Genetic dissection of Pax6 dosage requirements in the developing mouse eye.
Topics: Alleles; Animals; Cell Differentiation; Cornea; Eye Abnormalities; Eye Proteins; Gene Dosage; Genoty | 2005 |
Congenital hyperplastic persistent pupillary membranes: a conservative approach in management.
Topics: Adolescent; Eye Abnormalities; Female; Humans; Hyperplasia; Infant; Iris; Male; Membranes; Ophthalmo | 2005 |
Congenital microcoria associated with late-onset developmental glaucoma.
Topics: Adult; Basement Membrane; Connective Tissue; Cornea; Extracellular Matrix; Eye Abnormalities; Female | 2005 |
Rieger's anomaly and other ocular abnormalities in association with osteogenesis imperfecta and a COL1A1 mutation.
Topics: Abnormalities, Multiple; Adult; Atrophy; Collagen Type I; Collagen Type I, alpha 1 Chain; Corneal Ed | 2005 |
Bilateral complete isolated cryptophthalmos: a case report.
Topics: Abnormalities, Multiple; Ciliary Body; Eye Abnormalities; Eyelids; Female; Humans; Infant, Newborn; | 2005 |
Ocular pathologic features of Hermansky-Pudlak syndrome type 1 in an adult.
Topics: Adult; Astigmatism; Exotropia; Eye Abnormalities; Fatal Outcome; Fovea Centralis; Hermanski-Pudlak S | 2006 |
A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Case-Control Studies; Cell Count; Child; Child, Preschoo | 2006 |
Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformations.
Topics: Amino Acid Sequence; Anterior Eye Segment; Codon; DNA Mutational Analysis; Eye Abnormalities; Female | 2006 |
Congenital iris ectropion and glaucoma associated with intestinal neuronal dysplasia: a manifestation of a neural crest syndrome.
Topics: Child, Preschool; Enteric Nervous System; Eye Abnormalities; Glaucoma; Humans; Intestinal Diseases; | 2006 |
Ocular findings in Gillespie-like syndrome: association with a new PAX6 mutation.
Topics: Abnormalities, Multiple; Aniridia; Blepharoptosis; Child; DNA Mutational Analysis; Exotropia; Eye Ab | 2006 |
Genotype and phenotype correlations in congenital glaucoma: CYP1B1 mutations, goniodysgenesis, and clinical characteristics.
Topics: Anterior Chamber; Aryl Hydrocarbon Hydroxylases; Ciliary Body; Cytochrome P-450 CYP1B1; Cytochrome P | 2006 |
Progressive iris changes in a case of Axenfeld-Rieger syndrome.
Topics: Anterior Eye Segment; Eye Abnormalities; Female; Humans; Infant; Iris; Syndrome | 2006 |
Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.
Topics: Anterior Eye Segment; Antihypertensive Agents; Eye Abnormalities; Female; Filtering Surgery; Forkhea | 2007 |
Analyses of a novel L130F missense mutation in FOXC1.
Topics: Abnormalities, Multiple; Adult; Animals; Anterior Eye Segment; Cell Culture Techniques; Chlorocebus | 2007 |
Bilateral prominent schwalbe ring in the anterior chamber in a patient with axenfeld-rieger syndrome and megalocornea.
Topics: Abnormalities, Multiple; Adult; Anterior Chamber; Cornea; Eye Abnormalities; Glaucoma; Gonioscopy; H | 2007 |
Genotype and phenotype correlations in congenital glaucoma.
Topics: Anterior Chamber; Aryl Hydrocarbon Hydroxylases; Ciliary Body; Cytochrome P-450 CYP1B1; Cytochrome P | 2006 |
Hyperplastic persistent pupillary membranes with congenital corneal anomalies.
Topics: Adolescent; Consanguinity; Cornea; Corneal Topography; Eye Abnormalities; Female; Humans; Hyperplasi | 2007 |
Sectoral iris heterochromia and retinal pigment variation in 13q-syndrome.
Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, 13-15; Cytoge | 2007 |
Iridoschisis; a case report.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases; Uveitis, Intermediate | 1949 |
A FURTHER CASE OF IRIDOSCHISIS.
Topics: Eye Abnormalities; Humans; Iris; Iris Diseases | 1948 |
MICROCORNEA AND CONGENITAL COLOBOMA OF IRIS AND CHOROID IN ONE EYE WITH CONGENITAL GLAUCOMA AND CORNEAL OPACITY IN THE OTHER EYE.
Topics: Choroid; Coloboma; Cornea; Corneal Diseases; Corneal Opacity; Eye Abnormalities; Female; Functional | 1961 |
[Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].
Topics: Abnormalities, Multiple; Adult; Cornea; Craniofacial Abnormalities; Diagnostic Techniques, Ophthalmo | 2007 |
Persistent pupillary membranes in 3 siblings.
Topics: Child; Child, Preschool; Eye Abnormalities; Female; Humans; Iris; Male; Membranes; Mesoderm; Pigment | 2008 |
Deletion of G protein-coupled receptor 48 leads to ocular anterior segment dysgenesis (ASD) through down-regulation of Pitx2.
Topics: Animals; Anterior Eye Segment; Cataract; Cornea; Cyclic AMP Response Element-Binding Protein; Cyclic | 2008 |
A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomaly.
Topics: Abnormalities, Multiple; Anterior Eye Segment; Aryl Hydrocarbon Hydroxylases; Base Sequence; Cytochr | 2008 |
[Malformations of the eyeball: management].
Topics: Cornea; Eye; Eye Abnormalities; Humans; Iris; Lens, Crystalline; Pupil; Retina | 1983 |
[Peters' anomaly].
Topics: Anterior Chamber; Child, Preschool; Cornea; Eye Abnormalities; Female; Glaucoma; Humans; Infant; Iri | 1983 |
[Rieger's syndrome. Clinical and ultramicroscopy study].
Topics: Eye; Eye Abnormalities; Humans; Iris; Microscopy, Electron; Syndrome; Trabecular Meshwork | 1983 |
Ocular defects and short stature.
Topics: Adolescent; Agenesis of Corpus Callosum; Child; Child, Preschool; Coloboma; Encephalocele; Eye Abnor | 1980 |
A probable case of the homozygous condition of the aniridia gene.
Topics: Adrenal Glands; Adult; Eye Abnormalities; Female; Fetal Death; Genes, Dominant; Genes, Lethal; Genes | 1980 |
Ocular findings in arteriohepatic dysplasia (Alagille's syndrome).
Topics: Adult; Bile Ducts, Intrahepatic; Cardiovascular Diseases; Child, Preschool; Color Perception Tests; | 1981 |
[Ophthalmologic findings in trisomy 18 (Morbus Edwards) (author's transl)].
Topics: Chromosomes, Human, 16-18; Eye; Eye Abnormalities; Female; Humans; Infant, Newborn; Iris; Syndrome; | 1982 |
Ocular abnormalities in deletion of the long arm of chromosome 11.
Topics: Choroid; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, 6-12 | 1981 |
[Clinical picture and inheritance of ocular symptoms in arteriohepatic dysplasia (author's transl)].
Topics: Abnormalities, Multiple; Child; Child, Preschool; Diagnosis, Differential; Eye Abnormalities; Eye Di | 1982 |
Cardiac valvular disease and Axenfeld-Rieger syndrome.
Topics: Abnormalities, Multiple; Anterior Chamber; Aortic Valve Stenosis; Child; Eye Abnormalities; Glaucoma | 1994 |
Ocular anomalies in the alagille syndrome (arteriohepatic dysplasia).
Topics: Adult; Alagille Syndrome; Child; Cornea; Eye Abnormalities; Female; Humans; Hyperplasia; Infant, New | 1993 |
An unusual presentation of Smith-Magenis syndrome with iris dysgenesis.
Topics: Adult; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 17; DNA Probes; Eye Abnorma | 1996 |
Rieger anomaly and congenital glaucoma in the SHORT syndrome.
Topics: Abnormalities, Multiple; Child; Corneal Opacity; Eye Abnormalities; Facial Bones; Glaucoma; Humans; | 1996 |
Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.
Topics: Abnormalities, Multiple; Adult; Anterior Eye Segment; Chromosome Mapping; Chromosomes, Human, Pair 4 | 1996 |
Congenital eye malformations: a descriptive epidemiologic study in about one million newborns in Italy.
Topics: Anophthalmos; Cornea; Epidemiologic Factors; Eye Abnormalities; Female; Glaucoma; Humans; Infant, Ne | 1996 |
Focal dermal hypoplasia (Goltz's syndrome).
Topics: Abnormalities, Multiple; Adolescent; Brain; Choroid; Coloboma; Cornea; Eye Abnormalities; Female; Fo | 1997 |
Ocular abnormalities in a patient with partial deletion of chromosome 6p. A case report.
Topics: Abnormalities, Multiple; Chromosome Deletion; Chromosomes, Human, Pair 6; Corneal Opacity; Eye Abnor | 1997 |
Outcome of anterior-segment surgery in Rieger's anomaly.
Topics: Adolescent; Adult; Anterior Eye Segment; Child; Child, Preschool; Ciliary Body; Cryotherapy; Eye Abn | 1996 |
Menkes disease. New ocular and electroretinographic findings.
Topics: Electroretinography; Eye Abnormalities; Eyelashes; Humans; Infant; Iris; Male; Menkes Kinky Hair Syn | 1998 |
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.
Topics: Amino Acid Sequence; Animals; Base Sequence; Chromosome Mapping; Chromosomes, Human, Pair 6; DNA Pri | 1998 |
Ocular abnormalities in Alagille syndrome.
Topics: Abnormalities, Drug-Induced; Abnormalities, Multiple; Adolescent; Alagille Syndrome; Child; Child, P | 1999 |
Menkes disease.
Topics: Eye Abnormalities; Eyelashes; Humans; Iris; Menkes Kinky Hair Syndrome; Retinal Degeneration | 1999 |
Successful treatment of tractional corectopia using 2 mJ of energy with an Nd:YAG laser.
Topics: Eye Abnormalities; Female; Humans; Infant; Iris; Iris Diseases; Laser Therapy | 1999 |
Threading analysis of the Pitx2 homeodomain: predicted structural effects of mutations causing Rieger syndrome and iridogoniodysgenesis.
Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Animals; Calorimetry; Conserv | 1999 |
Trisomy 8p and Rieger malformation.
Topics: Chromosomes, Human, Pair 8; Eye Abnormalities; Humans; Infant; Iris; Male; Trisomy | 1998 |
Congenital iris ectropion associated with ocular albinism, foveal hypoplasia, and keratoconjunctivitis sicca.
Topics: Albinism, Ocular; Child, Preschool; Eye Abnormalities; Female; Fovea Centralis; Humans; Iris; Kerato | 1997 |
Phacoemulsification in eyes with a small pupil.
Topics: Adult; Aged; Aged, 80 and over; Cataract; Eye Abnormalities; Female; Humans; Iris; Male; Middle Aged | 2000 |
Unilateral glaucoma in Sotos syndrome (cerebral gigantism).
Topics: Abnormalities, Multiple; Brain; Cataract; Cornea; Eye Abnormalities; Gigantism; Glaucoma; Humans; In | 2000 |
SHORT syndrome: a case with high hyperopia and astigmatism.
Topics: Abnormalities, Multiple; Astigmatism; Child; Cornea; Corneal Opacity; Developmental Disabilities; Ey | 2000 |
Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Base Sequence; Cell Nucleus; DNA-Binding Prot | 2001 |
Rieger syndrome is associated with PAX6 deletion.
Topics: Abnormalities, Multiple; Anterior Eye Segment; Child; Chromosomes, Human, Pair 6; Eye Abnormalities; | 2001 |
Five cases of microphthalmia with other ocular malformations.
Topics: Abnormalities, Multiple; Cataract; Child, Preschool; Choroid; Coloboma; Corneal Opacity; Eye Abnorma | 2001 |
Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patients.
Topics: Adolescent; Amino Acid Sequence; Anterior Eye Segment; Base Sequence; Child; DNA Mutational Analysis | 2001 |
Infusion misdirection syndrome during trabeculectomy for primary trabeculodysgenesis.
Topics: Adult; Choroid Hemorrhage; Cornea; Eye Abnormalities; Female; Humans; Intraocular Pressure; Intraope | 2002 |
Fibrous congenital iris membranes with pupillary distortion.
Topics: Anterior Eye Segment; Eye Abnormalities; Female; Fibrosis; Glaucoma, Angle-Closure; Humans; Infant; | 2001 |
Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from Brazil.
Topics: Brazil; Chromosomes, Human, Pair 4; Chromosomes, Human, Pair 6; Cornea; DNA Mutational Analysis; DNA | 2002 |
Clinical and ultrastructural features of a novel hereditary anterior segment dysgenesis.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anterior Eye Segment; Cataract; Cornea; Corneal Stroma; | 2002 |
A goniolens for clinical monitoring of the mouse iridocorneal angle and optic nerve.
Topics: Animals; Anterior Eye Segment; Ciliary Body; Cornea; Equipment Design; Eye Abnormalities; Glaucoma; | 2002 |
Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.
Topics: Base Sequence; Chromosome Deletion; Chromosomes, Human, Pair 6; Contig Mapping; Cornea; DNA-Binding | 2002 |
Ophthalmic features of chromosome deletion 4p- (Wolf-Hirschhorn syndrome).
Topics: Abnormalities, Multiple; Adolescent; Adult; Azure Stains; Blepharoptosis; Chromosome Deletion; Chrom | 1978 |
Dysgenetic lens (dyl)--a new gene in the mouse.
Topics: Animals; Cataract; Corneal Opacity; Eye; Eye Abnormalities; Female; Genes, Recessive; Heterozygote; | 1979 |
Congenital nonprogressive facial hemiatrophy with ipsilateral eye abnormalities and juvenile glaucoma.
Topics: Animals; Child; Diabetes Mellitus, Type 1; Eye Abnormalities; Facial Hemiatrophy; Female; Glaucoma; | 1979 |
Rieger's anomaly with congenital glaucoma a case presentation of postnatal anterior segment maturation.
Topics: Abnormalities, Multiple; Acetazolamide; Adult; Eye Abnormalities; Female; Glaucoma; Humans; Infant; | 1979 |
Vascular anastomoses between the iris and persistent hyperplastic primary vitreous.
Topics: Abnormalities, Multiple; Adult; Child, Preschool; Diagnosis, Differential; Eye Abnormalities; Eye Di | 1979 |
Angle-closure glaucoma in nanophthalmos.
Topics: Choroid; Eye Abnormalities; Female; Glaucoma; Humans; Iris; Laser Therapy; Middle Aged; Retinal Deta | 1979 |
Down's syndrome: a ten-year group study.
Topics: Adolescent; Adult; Blepharitis; Child; Conjunctivitis; Down Syndrome; Eye Abnormalities; Eye Disease | 1977 |
Cytogenetic investigation of cat-eye syndrome.
Topics: Adult; Anus, Imperforate; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chr | 1977 |
Ocular findings in triploidy.
Topics: Abnormalities, Multiple; Adolescent; Cataract; Chromosome Aberrations; Chromosome Disorders; Colobom | 1977 |
[Therapeutic results in 45 children with congenital glaucoma].
Topics: Abnormalities, Multiple; Child; Child, Preschool; Ciliary Body; Evaluation Studies as Topic; Eye Abn | 1975 |
Glaucoma--a classic treatise--part 5.
Topics: Abnormalities, Multiple; Adrenal Cortex Hormones; Child; Eye Abnormalities; Eye Diseases; Eye Injuri | 1976 |
The surgery of cataracts in children.
Topics: Atropine; Cataract Extraction; Cyclopentolate; Drainage; Eye Abnormalities; Humans; Infant; Iris | 1976 |
Malformation syndromes. A selected miscellany.
Topics: Abnormalities, Multiple; Adolescent; Child; Child, Preschool; Chromosomes, Human, 6-12 and X; Dental | 1975 |
A low birthweight syndrome, ? Rieger syndrome.
Topics: Abnormalities, Multiple; Child, Preschool; Eye Abnormalities; Female; Humans; Infant, Newborn; Infan | 1975 |
[Corneal ectaxy and cataract in dysgenesis mesodermalis cornea and iridis (Rieger)].
Topics: Adult; Cataract; Cornea; Corneal Diseases; Eye Abnormalities; Humans; Iris; Male | 1976 |
Bilateral renal agenesis with multiple congenital ocular anomalies.
Topics: Abnormalities, Multiple; Anterior Chamber; Cataract; Cornea; Eye Abnormalities; Humans; Infant, Newb | 1976 |
Russell-Silver dwarfism.
Topics: Cataract; Child; Cornea; Dwarfism, Pituitary; Eye Abnormalities; Eye Movements; Glaucoma; Humans; In | 1976 |
[Hypoplasia of the pulmonary artery in Rieger's Syndrome (author's transl)].
Topics: Abnormalities, Multiple; Angiocardiography; Child; Cineangiography; Eye Abnormalities; Female; Human | 1976 |
Ectopia lentis et pupillae: the genetic aspects and differential diagnosis.
Topics: Adult; Child; Child, Preschool; Diagnosis, Differential; Ectopia Lentis; Eye Abnormalities; Genes, R | 1991 |
[Late complications in patients with intraocular lenses].
Topics: Eye Abnormalities; Humans; Iris; Lens Subluxation; Lenses, Intraocular; Postoperative Complications; | 1990 |
[Fluorescein angiography of the iris in pseudophakia].
Topics: Aged; Eye Abnormalities; Female; Fluorescein Angiography; Humans; Iris; Iris Diseases; Lenses, Intra | 1990 |
Familial Wolf-Hirschhorn syndrome associated with Rieger anomaly of the eye.
Topics: Abnormalities, Multiple; Chromosomes, Human, Pair 10; Chromosomes, Human, Pair 4; Eye Abnormalities; | 1990 |
[Dysgenesis of the neural crest, ectoderm, mesoderm and fetal alcohol syndrome].
Topics: Abnormalities, Multiple; Adolescent; Anterior Chamber; Ectodermal Dysplasia; Eye Abnormalities; Fema | 1990 |
Usual and unusual uses of the laser in glaucoma.
Topics: Ciliary Body; Cysts; Eye Abnormalities; Glaucoma; Humans; Iris; Iris Diseases; Laser Therapy; Light | 1985 |
Peters' anomaly as a consequence of genetic and nongenetic syndromes.
Topics: Abnormalities, Multiple; Child, Preschool; Cornea; Corneal Transplantation; Eye; Eye Abnormalities; | 1986 |
Additional eye findings in a girl with the velo-cardio-facial syndrome.
Topics: Abnormalities, Multiple; Child; Coloboma; Eye Abnormalities; Facial Asymmetry; Female; Heart Defects | 1986 |
Aniridia, atypical iris defects, optic pit and the morning glory disc anomaly in a family.
Topics: Abnormalities, Multiple; Eye Abnormalities; Female; Humans; Infant; Iris; Optic Disk | 1986 |
Ocular coloboma associated with a solitary maxillary central incisor and growth failure: manifestations of holoprosencephaly.
Topics: Abnormalities, Multiple; Cataract; Choroid; Coloboma; Eye Abnormalities; Growth Disorders; Humans; I | 1987 |
Congenital corneal opacity (Peters' anomaly) combined with buphthalmos and aniridia.
Topics: Cornea; Corneal Opacity; Eye Abnormalities; Humans; Iris; Karyotyping; Male | 1985 |
Ultrasonographic visualization of the fetal eye.
Topics: Eye Abnormalities; Female; Humans; Iris; Microcephaly; Microphthalmos; Pregnancy; Prenatal Diagnosis | 1985 |
[An unexplained syndrom with eye and tooth defects (author's transl)].
Topics: Abnormalities, Multiple; Adolescent; Adult; Corneal Opacity; Dental Enamel Hypoplasia; DMF Index; Ey | 1974 |
Minor ocular abnormalities associated with thalidomide.
Topics: Abnormalities, Drug-Induced; Child, Preschool; Choroid; Eye Abnormalities; Female; Humans; Infant; I | 1966 |
Hyaline corneal opacities in a case of Rieger's anomaly.
Topics: Abnormalities, Multiple; Child; Cornea; Corneal Opacity; Descemet Membrane; Eye Abnormalities; Femal | 1969 |
The ocular manifestations of congenital rubella.
Topics: Cataract; Child; Child, Preschool; Ciliary Body; Cornea; Eye Abnormalities; Eye Manifestations; Fema | 1972 |
Agenesis of the corpus callosum in the median facial cleft syndrome and associated ocular malformations.
Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Coloboma; Cornea; Craniofacial Dysostosis; Ecz | 1973 |
Arhinencephaly unilateralis, uveal coloboma, and lens reduplication.
Topics: Abnormalities, Multiple; Child; Child, Preschool; Choroid; Ciliary Body; Coloboma; Craniofacial Dyso | 1974 |
Ocular histopathology of Norrie's disease.
Topics: Abnormalities, Multiple; Blindness; Eye; Eye Abnormalities; Genes, Recessive; Hearing Disorders; Hum | 1974 |
The cat eye syndrome.
Topics: Anus, Imperforate; Body Weight; Cephalometry; Chromosome Aberrations; Chromosome Disorders; Chromoso | 1974 |
Autosomal dominant transmission of isolated growth hormone deficiency in iris-dental dysplasia (Rieger's syndrome).
Topics: Abnormalities, Multiple; Adolescent; Adult; Agenesis of Corpus Callosum; Anencephaly; Blood Glucose; | 1974 |
Ocular manifestations of Conradi disease.
Topics: Cataract; Chondrodysplasia Punctata; Eye Abnormalities; Eye Diseases; Eye Manifestations; Eyelids; H | 1974 |
[Malformations of the eye and associated structures, and their treatment].
Topics: Albinism; Blepharoptosis; Cataract; Coloboma; Craniofacial Dysostosis; Eye Abnormalities; Eye Diseas | 1974 |
Congenital corneal opacities in a patient with Rieger's anomaly and Down's syndrome.
Topics: Abnormalities, Multiple; Aged; Cornea; Corneal Opacity; Down Syndrome; Eye Abnormalities; Female; Gl | 1968 |
Ocular changes in simple trisomy and in a few cases of partial trisomy.
Topics: Abnormalities, Multiple; Adolescent; Cataract; Child; Child, Preschool; Chromosome Aberrations; Chro | 1968 |
Persistent hyperplastic primary vitreous. Cases in Denmark 1942-1966. A mainly histopathological study.
Topics: Abnormalities, Multiple; Adolescent; Adult; Child; Child, Preschool; Ciliary Body; Denmark; Eye; Eye | 1968 |
[Rôle of the optic cupula and the crystalline lens in ocular morphogenesis: teratogenic arguments].
Topics: Animals; Eye; Eye Abnormalities; Humans; Iris; Lens, Crystalline; Rabbits | 1973 |
[Congenital glaucoma-juvenile glaucoma].
Topics: Abnormalities, Multiple; Adolescent; Adult; Age Factors; Cornea; Corneal Opacity; Diagnosis, Differe | 1974 |
[Multiple abnormalities resembling Apert's syndrome].
Topics: Abnormalities, Multiple; Child; Cleft Lip; Cleft Palate; Clubfoot; Craniofacial Dysostosis; Diagnosi | 1969 |
Dominant goniodysgenesis with late congenital glaucoma. A re-examination of Berg's pedigree.
Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorder | 1972 |
[Operation for senile cataract in eyes with congenital coloboma of the uvea].
Topics: Aged; Cataract Extraction; Chymotrypsin; Coloboma; Eye Abnormalities; Female; Follow-Up Studies; Hum | 1972 |
Ocular manifestations of the Meckel syndrome.
Topics: Abnormalities, Multiple; Anophthalmos; Cataract; Cornea; Craniofacial Dysostosis; Diseases in Twins; | 1972 |
Ocular anomalies in trisomy 13-15: an analysis of 13 eyes with two new findings.
Topics: Abnormalities, Multiple; Adult; Anterior Chamber; Cartilage; Chromosomes, Human, 13-15; Coloboma; Co | 1972 |
[Ocular malformations in a case of crying cat syndrome].
Topics: Abnormalities, Multiple; Cri-du-Chat Syndrome; Cytogenetics; Eye Abnormalities; Female; Humans; Infa | 1972 |
S survey of ocular findings in 16- to 24-week-old beagles.
Topics: Animals; Corneal Opacity; Dog Diseases; Dogs; Eye Abnormalities; Eye Diseases; Eyelashes; Female; Ir | 1973 |
Anterior chamber cleavage syndrome. A typical case of Peters' anomaly with primary aphakia.
Topics: Abnormalities, Multiple; Anterior Chamber; Cornea; Corneal Opacity; Descemet Membrane; Eye Abnormali | 1972 |
Iris dysplasia, orbital hypertelorism, and psychomotor retardation: a dominantly inherited developmental syndrome.
Topics: Abnormalities, Multiple; Adult; Brain; Child, Preschool; Craniofacial Dysostosis; Eye Abnormalities; | 1973 |
Bilateral oro-ocular cleft. Case report.
Topics: Abnormalities, Multiple; Choroid; Cleft Palate; Coloboma; Eye Abnormalities; Face; Female; Humans; I | 1973 |
[Agenesis of the corpus callosum, median facial fissure syndrome, and eye malformations].
Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Choroid; Coloboma; Cornea; Craniofacial Dysost | 1972 |
Acquired corneal dystrophy; dysgenesis of the anterior segment of the eye, blue scleral band, oligodontia, and metacarpal dysplasia (dysplasia oculo-dento-digitalis?).
Topics: Adolescent; Cornea; Corneal Dystrophies, Hereditary; Descemet Membrane; Eye Abnormalities; Female; G | 1965 |
Inherited variation in Rieger's malformation.
Topics: Adult; Aged; Child; Coloboma; Cornea; Eye Abnormalities; Female; Humans; Iris; Male; Middle Aged | 1965 |
Ocular manifestations of congenital rubella syndrome. Recovery of virus from affected infants.
Topics: Cataract; Eye Abnormalities; Female; Humans; In Vitro Techniques; Infant, Newborn; Infant, Newborn, | 1966 |
[A rare dysplasia: the oculo-dento-digital syndrome].
Topics: Cerebral Ventriculography; Child; Dental Enamel Hypoplasia; Electroencephalography; Epilepsy; Eye Ab | 1965 |
Ocular manifestations of the 1964-65 rubella epidemic.
Topics: Cataract; Connecticut; Cornea; Corneal Opacity; Eye Abnormalities; Eye Diseases; Female; Glaucoma; H | 1967 |
Congenital eye defects on rats following maternal folic-acid deficiency during pregnancy.
Topics: Animals; Cell Differentiation; Choroid; Ciliary Body; Cornea; Embryo, Mammalian; Eye; Eye Abnormalit | 1966 |
Color dilution and hereditary defects in collie dogs.
Topics: Animals; Blindness; Deafness; Dog Diseases; Dogs; Ear; Eye Abnormalities; Fundus Oculi; Genes; Hair; | 1967 |
Unilateral microcornea and enophthalmos with bilateral anterior and posterior anomalies.
Topics: Child; Choroid; Coloboma; Cornea; Eye Abnormalities; Female; Humans; Iris; Microphthalmos; Myopia; P | 1967 |
[Congenital spherophakia as a cause of severe myopia].
Topics: Child; Child, Preschool; Ectropion; Eye Abnormalities; Female; Humans; Infant; Iris; Lens, Crystalli | 1964 |
[Clinical and electronystagmographic study of 50 subjects with so-called "congenital" nystagmus].
Topics: Adolescent; Adult; Albinism; Cataract; Child; Child, Preschool; Coloboma; Electrooculography; Eye Ab | 1968 |
[Clinico-therapeutic considerations on some cases of congenital malformations of the iris and on their complications].
Topics: Adolescent; Adult; Cataract; Child; Child, Preschool; Coloboma; Corneal Dystrophies, Hereditary; Eye | 1966 |
Congenital mesodermal anomalies and glaucoma.
Topics: Abnormalities, Multiple; Cornea; Eye Abnormalities; Fingers; Glaucoma; Hand Deformities, Congenital; | 1968 |
Spontaneous retinal ablation in a case with congenital anomalities of the eye.
Topics: Child; Coloboma; Eye Abnormalities; Fundus Oculi; Humans; Iris; Lens, Crystalline; Male; Retinal Det | 1968 |
[The surgical treatment of glaucoma in Rieger's anomaly].
Topics: Adult; Anterior Chamber; Cornea; Eye Abnormalities; Glaucoma; Humans; Iris; Male | 1966 |
[Eye abnormalities of a child with an extra chromosome fragment].
Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Coloboma; E | 1968 |
[Congenital glaucoma with dominant heredity associated with ocular and somatic malformations (Rieger's syndrome)].
Topics: Abnormalities, Multiple; Adolescent; Adult; Child; Child, Preschool; Cleft Palate; Corneal Opacity; | 1968 |
Cataract extraction in a case of congenital coloboma of the iris.
Topics: Cataract Extraction; Coloboma; Eye Abnormalities; Female; Humans; Intraocular Pressure; Iris; Middle | 1968 |
[Circumpupillary aplasia of the iris. (Case report)].
Topics: Blepharoptosis; Cataract; Child; Child, Preschool; Coloboma; Eye Abnormalities; Female; Humans; Infa | 1967 |
[An atypical case of tapeto-retinal degeneration associated with coloboma of the iris and with whitish foci in the lower retinal quadrants].
Topics: Adult; Choroid; Coloboma; Eye Abnormalities; Eye Diseases; Humans; Iris; Male; Retina; Retinal Degen | 1967 |
Anomalies of the eyes in descendants of women, irradiated with small X-ray doses during age of fertility.
Topics: Adolescent; Adult; Atrophy; Choroid; Coloboma; Eye Abnormalities; Female; Fetus; Humans; Iris; Male; | 1968 |
Intraocular cartilage in a microphthalmic eye of an otherwise healthy girl.
Topics: Abnormalities, Multiple; Adipose Tissue; Cartilage; Ciliary Body; Coloboma; Eye; Eye Abnormalities; | 1969 |
Ocular defects associated with homocystinuria.
Topics: Eye Abnormalities; Eye Diseases; Female; Homocystinuria; Humans; Intellectual Disability; Iris; Lens | 1969 |
[Iridoschisis in a girl with karyotype 48 XXXX].
Topics: Child; Coloboma; Dermatoglyphics; Eye Abnormalities; Female; Humans; Intellectual Disability; Iris; | 1969 |
[The current status of the problem of implantation of intraocular lenses and intracorneal implants].
Topics: Acrylates; Albinism; Anterior Chamber; Cataract Extraction; Coloboma; Cornea; Diplopia; Eye Abnormal | 1969 |
[Cranio-facial malformations and congenital aniridia in the same family].
Topics: Adult; Eye Abnormalities; Female; Head; Humans; Infant, Newborn; Iris; Male | 1968 |
Colobomatous malformations of the ocular globe.
Topics: Anophthalmos; Choroid; Coloboma; Congenital Abnormalities; Eye Abnormalities; Genes, Dominant; Genes | 1968 |
[Coloboma of iris and choroid in a patient with XYY-syndrome].
Topics: Abnormalities, Multiple; Adult; Choroid; Coloboma; Eye Abnormalities; Humans; Iris; Juvenile Delinqu | 1970 |
[Iridoschisis: 3 cases].
Topics: Aged; Coloboma; Eye Abnormalities; Female; Humans; Iris; Middle Aged | 1968 |
Ocular pathology of Patau's syndrome with an unbalanced D-D translocation.
Topics: Abnormalities, Multiple; Anterior Chamber; Autopsy; Chromosomes, Human, 1-3; Chromosomes, Human, 13- | 1970 |
[Association of an iris and lens coloboma with a concentric narrowing of the color visual field].
Topics: Adult; Coloboma; Color Perception; Congenital Abnormalities; Eye Abnormalities; Humans; Iris; Lens, | 1970 |
[On an unusual form of atypical coloboma of the iris (triangular dyscoria)].
Topics: Coloboma; Eye Abnormalities; Female; Humans; Iris; Middle Aged | 1969 |
Developmental factor in the etiopathogenesis of glaucomatocyclitic crisis.
Topics: Adult; Anterior Chamber; Eye Abnormalities; Glaucoma; Humans; Iris; Male; Uveitis, Anterior | 1970 |
[A case of atypical Marfan's syndrome with epilepsy, oligophrenia and coloboma of the iris].
Topics: Adult; Coloboma; Electrocardiography; Electroencephalography; Epilepsy, Tonic-Clonic; Eye Abnormalit | 1969 |
[Frequent familial occurrence of a multiplex malformation of the eye].
Topics: Abnormalities, Multiple; Adult; Blepharoptosis; Child; Child, Preschool; Chromosome Aberrations; Chr | 1971 |
Colobomas in non-human primates.
Topics: Animals; Choroid; Coloboma; Congenital Abnormalities; Eye; Eye Abnormalities; Haplorhini; Hominidae; | 1971 |
Uveal colobomata and other anomalies in three generations of one family.
Topics: Abnormalities, Multiple; Adult; Blepharoptosis; Child, Preschool; Cleft Lip; Cleft Palate; Coloboma; | 1971 |
Ocular colobomas in domestic cats.
Topics: Animals; Cat Diseases; Cats; Choroid; Coloboma; Congenital Abnormalities; Eye Abnormalities; Eyelids | 1971 |
[Progressive iris atrophy and iridosohisis].
Topics: Age Factors; Aged; Coloboma; Eye Abnormalities; Humans; Iris; Male; Sex Factors | 1971 |
Inter-oculo-irido-auditory dysplasia. (Waardenburg, van der Hoeve, Halberstsma syndrome).
Topics: Abnormalities, Multiple; Child; Deafness; Egypt; Eye Abnormalities; Female; Humans; Iris; Osteogenes | 1971 |
Ocular pathology of Trisomy 18.
Topics: Abnormalities, Multiple; Chromatin; Chromosomes, Human, 16-18; Cornea; Descemet Membrane; Epithelium | 1971 |
Mesoectodermal dysplasia of the iris and cornea, mental retardation and myopathy: a sporadic case.
Topics: Abnormalities, Multiple; Cornea; Ectodermal Dysplasia; Eye Abnormalities; Humans; Intellectual Disab | 1971 |