2-propanol has been researched along with Eye Diseases, Hereditary in 43 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 Diseases, Hereditary: Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
| Excerpt | Relevance | Reference |
|---|---|---|
| "iris melanoma) is paramount." | 2.55 | [Diagnosis and Therapy of Iris Lesions]. ( Heindl, LM; Koch, KR; Mor, JM, 2017) |
| "Epithelial cysts run a high risk of recurrence and conversion to sheet-like ingrowth after surgical intervention." | 1.62 | Long-term outcomes of "open iridectomy" for secondary anterior chamber epithelial iris cysts. ( Guo, X; Huang, Y; Kong, Q; Lan, J; Liu, T; Pan, X; Wei, Y; Xie, L; Xie, P, 2021) |
| "Aniridia is a rare panocular disorder characterized by iris hypoplasia and other associated eye anomalies." | 1.42 | Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia. ( Dubey, SK; Mahalaxmi, N; Sundaresan, P; Vijayalakshmi, P, 2015) |
| "The mean size of total cysts was (0." | 1.38 | Effect of primary iris and ciliary body cyst on anterior chamber angle in patients with shallow anterior chamber. ( Wang, BH; Yao, YF, 2012) |
| "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) |
| "Rieger syndrome is an autosomal dominant condition characterized by a variable combination of anterior segment dysgenesis, dental anomalies, and umbilical hernia." | 1.31 | Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations. ( Black, GC; Churchill, A; Clayton-Smith, J; Hanson, I; Kerr, B; Lloyd, IC; McKeown, C; Perveen, R; Super, M; Taylor, D; van Heyningen, V; Winter, R, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (9.30) | 18.7374 |
| 1990's | 4 (9.30) | 18.2507 |
| 2000's | 9 (20.93) | 29.6817 |
| 2010's | 19 (44.19) | 24.3611 |
| 2020's | 7 (16.28) | 2.80 |
| Authors | Studies |
|---|---|
| Jacobson, A | 1 |
| Bohnsack, BL | 1 |
| Guillemin, M | 1 |
| Blanc, J | 1 |
| Baudin, F | 1 |
| Haddad, D | 1 |
| Bron, AM | 1 |
| Creuzot-Garcher, C | 1 |
| Mc Glacken-Byrne, AB | 1 |
| Prentice, D | 1 |
| Roshandel, D | 1 |
| Brown, MR | 1 |
| Tuch, P | 1 |
| Yau, KS | 1 |
| Sivadorai, P | 1 |
| Davis, MR | 1 |
| Laing, NG | 1 |
| Chen, FK | 1 |
| Tabuenca Del Barrio, L | 1 |
| Mozo Cuadrado, M | 1 |
| Gonzalvo Ibáñez, FJ | 1 |
| Plaza Ramos, P | 1 |
| Zubicoa Enériz, A | 1 |
| Boese, EA | 1 |
| Critser, DB | 1 |
| Fingert, JH | 1 |
| Arestova, NN | 1 |
| Kalinichenko, RV | 1 |
| Egiyan, NS | 1 |
| Kruglova, TB | 1 |
| Lan, J | 1 |
| Liu, T | 1 |
| Huang, Y | 1 |
| Pan, X | 1 |
| Wei, Y | 1 |
| Xie, P | 1 |
| Kong, Q | 1 |
| Guo, X | 1 |
| Xie, L | 1 |
| Solheim, MH | 1 |
| Clermont, AC | 1 |
| Winnay, JN | 1 |
| Hallstensen, E | 1 |
| Molven, A | 1 |
| Njølstad, PR | 1 |
| Rødahl, E | 2 |
| Kahn, CR | 1 |
| Chang, TC | 1 |
| Bauer, M | 1 |
| Puerta, HS | 1 |
| Greenberg, MB | 1 |
| Cavuoto, KM | 1 |
| Mor, JM | 1 |
| Koch, KR | 1 |
| Heindl, LM | 1 |
| Bengarai, W | 1 |
| Chokrani, H | 1 |
| Berraho, A | 1 |
| Taubenslag, KJ | 1 |
| Scanga, HL | 1 |
| Huey, J | 1 |
| Lee, J | 1 |
| Medsinge, A | 1 |
| Sylvester, CL | 1 |
| Cheng, KP | 1 |
| Nischal, KK | 2 |
| Torrado, LA | 1 |
| Ho, ML | 1 |
| Brodsky, MC | 1 |
| Galvis, V | 1 |
| Tello, A | 1 |
| Rangel, CM | 1 |
| Carreño, NI | 1 |
| Berrospi, RD | 1 |
| Niño, CA | 1 |
| Morlino, S | 1 |
| Alesi, V | 1 |
| Calì, F | 1 |
| Lepri, FR | 1 |
| Secinaro, A | 1 |
| Grammatico, P | 1 |
| Novelli, A | 1 |
| Drago, F | 1 |
| Castori, M | 1 |
| Baban, A | 1 |
| Shakrawal, J | 1 |
| Selvan, H | 2 |
| Sharma, A | 2 |
| Angmo, D | 2 |
| Kumar, V | 1 |
| Padhy, SK | 1 |
| Nasser, LS | 1 |
| Paranaíba, LM | 1 |
| Frota, AC | 1 |
| Gomes, A | 1 |
| Versiani, G | 1 |
| Martelli Júnior, H | 1 |
| Léonard, A | 1 |
| De Potter, P | 1 |
| López-Arroquia, TE | 1 |
| Avendaño-Cantos, EM | 1 |
| Mesa-Varona, D | 1 |
| Gálvez-Martínez, J | 1 |
| López-Romero, S | 1 |
| Nuñez-Plascencia, R | 1 |
| González del Valle, F | 1 |
| Handor, H | 1 |
| Laghmari, M | 1 |
| Hafidi, Z | 1 |
| Daoudi, C | 1 |
| Daoudi, R | 1 |
| Dubey, SK | 1 |
| Mahalaxmi, N | 1 |
| Vijayalakshmi, P | 1 |
| Sundaresan, P | 1 |
| Chen, CJ | 1 |
| Kaufman, S | 1 |
| Packo, K | 1 |
| Stöhr, H | 1 |
| Weber, BH | 1 |
| Goldberg, MF | 1 |
| Coppens, G | 1 |
| Zeyen, T | 1 |
| Wang, BH | 1 |
| Yao, YF | 1 |
| Hwang, JM | 1 |
| Chung, DC | 1 |
| Traboulsi, EI | 1 |
| WEEKERS, R | 1 |
| WATILLON, M | 1 |
| FRANDSEN, E | 1 |
| PRIMROSE, JA | 1 |
| HENKIND, P | 1 |
| SIGEL, IM | 1 |
| CARR, RE | 1 |
| Berges, O | 1 |
| Stefaniu, I | 1 |
| Chiotoroiu, S | 1 |
| Epure, C | 1 |
| Frasia, M | 1 |
| Llinas, A | 1 |
| Dorairaj, S | 1 |
| Liebmann, JM | 1 |
| Ritch, R | 2 |
| Kamińska, A | 1 |
| Sokołowska-Oracz, A | 1 |
| Pawluczyk-Dyjecińska, M | 1 |
| Szaflik, JP | 1 |
| Bredrup, C | 1 |
| Knappskog, PM | 1 |
| Boman, H | 1 |
| Dietlein, TS | 1 |
| Jacobi, PC | 1 |
| Krieglstein, GK | 1 |
| John, SW | 1 |
| Smith, RS | 1 |
| Savinova, OV | 1 |
| Hawes, NL | 1 |
| Chang, B | 1 |
| Turnbull, D | 1 |
| Davisson, M | 1 |
| Roderick, TH | 1 |
| Heckenlively, JR | 1 |
| Byles, DB | 1 |
| Cheng, H | 1 |
| Perveen, R | 1 |
| Lloyd, IC | 1 |
| Clayton-Smith, J | 1 |
| Churchill, A | 1 |
| van Heyningen, V | 1 |
| Hanson, I | 1 |
| Taylor, D | 1 |
| McKeown, C | 1 |
| Super, M | 1 |
| Kerr, B | 1 |
| Winter, R | 1 |
| Black, GC | 1 |
| Singerman, LJ | 1 |
| Mittra, RA | 1 |
| Akpek, EK | 1 |
| Jun, AS | 1 |
| Goodman, DF | 1 |
| Green, WR | 1 |
| Gottsch, JD | 1 |
3 reviews available for 2-propanol and Eye Diseases, Hereditary
| Article | Year |
|---|---|
[Diagnosis and Therapy of Iris Lesions].
Topics: Diagnosis, Differential; Diagnostic Imaging; Eye Diseases, Hereditary; Humans; Iris; Iris Diseases; | 2017 |
[Applications of noninvasive high-resolution ultrasound imaging in ophthalmology].
Topics: Ciliary Body; Cornea; Eye; Eye Diseases; Eye Diseases, Hereditary; Female; Humans; Infant; Iris; Mal | 2006 |
A unification hypothesis of pigment dispersion syndrome.
Topics: Animals; Exfoliation Syndrome; Eye Diseases, Hereditary; Female; Humans; Iris; Male; Philosophy; Ult | 1996 |
40 other studies available for 2-propanol and Eye Diseases, Hereditary
| Article | Year |
|---|---|
Anterior megalophthalmos in sisters with Witteveen-Kolk syndrome.
Topics: Eye Abnormalities; Eye Diseases, Hereditary; Female; Genetic Diseases, X-Linked; Humans; Hydrophthal | 2022 |
[Bilateral peripupillary cysts in a 30 year-old patient].
Topics: Adult; Eye Diseases, Hereditary; Humans; Iris; Male; Photography; Pigment Epithelium of Eye; Tomogra | 2020 |
High-resolution iris and retinal imaging in multisystemic smooth muscle dysfunction syndrome due to a novel Asn117Lys substitution in ACTA2: a case report.
Topics: Actins; Adult; Aged; Amino Acid Substitution; Cerebrovascular Disorders; Ductus Arteriosus, Patent; | 2020 |
Free-floating iris cyst.
Topics: Adult; Eye Diseases, Hereditary; Female; Humans; Iris; Iris Diseases; Movement; Ophthalmologic Surgi | 2020 |
High Iris Insertion in Axenfeld-Rieger Syndrome.
Topics: Adult; Anterior Eye Segment; Cornea; Eye Abnormalities; Eye Diseases, Hereditary; Gonioscopy; Humans | 2020 |
[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 |
Long-term outcomes of "open iridectomy" for secondary anterior chamber epithelial iris cysts.
Topics: Adolescent; Adult; Aftercare; Anterior Chamber; Child; Child, Preschool; Eye Diseases, Hereditary; E | 2021 |
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 |
Axenfeld-Rieger syndrome.
Topics: Abnormalities, Multiple; Anterior Eye Segment; Cataract; Child; Ectropion; Eye Abnormalities; Eye Di | 2018 |
Iris anomalies and the incidence of
Topics: Actins; Child, Preschool; DNA; DNA Mutational Analysis; Eye Diseases, Hereditary; Female; Follow-Up | 2019 |
Posterior Embryotoxon, Corectopia, and Cerebellar Dysgenesis.
Topics: Abnormalities, Multiple; Adolescent; Anterior Eye Segment; Cerebellum; Eye Abnormalities; Eye Diseas | 2018 |
Iris-clip versus iris-claw intraocular lenses.
Topics: Cataract; Eye Diseases, Hereditary; Follow-Up Studies; Genetic Diseases, X-Linked; Humans; Iris; Len | 2018 |
LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant.
Topics: Adolescent; Child; Corneal Diseases; Ectopia Lentis; Eye Diseases, Hereditary; Female; Genetic Disea | 2019 |
Double trouble: Microspherophakia with Axenfeld-Rieger anomaly.
Topics: Abnormalities, Multiple; Adolescent; Anterior Chamber; Anterior Eye Segment; Corneal Diseases; Ectop | 2019 |
Familial exudative vitreoretinopathy in a patient with choroidal coloboma.
Topics: Angiogenesis Inhibitors; Bevacizumab; Child; Choroid; Coloboma; Eye Diseases, Hereditary; Familial E | 2019 |
The Missing Mesenchyme Captured-Axenfeld-Rieger Anomaly.
Topics: Anterior Eye Segment; Eye Abnormalities; Eye Diseases, Hereditary; Humans; Iris; Mesoderm | 2019 |
[Waardenburg syndrome--ophthalmic findings and criteria for diagnosis: case reports].
Topics: Adult; Child, Preschool; Eye Diseases, Hereditary; Female; Genetic Predisposition to Disease; Humans | 2012 |
[Partially pigmented vitreous cyst].
Topics: Eye Diseases, Hereditary; Humans; Iris; Male; Middle Aged; Pigment Epithelium of Eye; Ultrasonograph | 2013 |
Amblyopia secondary to iris cyst.
Topics: Amblyopia; Astigmatism; Cataract; Child, Preschool; Eye Diseases, Hereditary; Humans; Iris; Male; Mi | 2014 |
[Iris atrophy in a case of Rieger's anomaly].
Topics: Anterior Eye Segment; Atrophy; Child, Preschool; Eye Abnormalities; Eye Diseases, Hereditary; Humans | 2014 |
Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia.
Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Aniridia; Base Sequence; Case-Control Studies; Catarac | 2015 |
Long-Term Macular Changes in the First Proband of Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Due to a Newly Identified Mutation in BEST1.
Topics: Adult; Atrophy; Bestrophins; Blindness; Chloride Channels; Choroid Diseases; Exons; Eye Diseases, He | 2016 |
Axenfeld's anomaly.
Topics: Abnormalities, Multiple; Adult; Anterior Eye Segment; Eye Abnormalities; Eye Diseases, Hereditary; F | 2010 |
Effect of primary iris and ciliary body cyst on anterior chamber angle in patients with shallow anterior chamber.
Topics: Adult; Anterior Chamber; Ciliary Body; Cysts; Eye Diseases, Hereditary; Female; Humans; Iris; Iris D | 2012 |
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 |
[Congenital glaucoma without megalocornea; clinical studies].
Topics: Child; Eye Diseases, Hereditary; Genetic Diseases, X-Linked; Glaucoma; Humans; Infant; Iris | 1957 |
RIEGER'S SYNDROME COMBINED WITH OLIGODONITIA AND FINGER DEFORMITY.
Topics: Anterior Chamber; Anterior Eye Segment; Child; Congenital Abnormalities; Cornea; Eye Abnormalities; | 1963 |
PSEUDOPAPILLOEDEMA AND PSEUDONEURITIS.
Topics: Adolescent; Child; Diagnosis; Eye Diseases, Hereditary; Humans; Iris; Neuritis; Optic Nerve Diseases | 1965 |
MESODERMAL DYSGENESIS OF THE ANTERIOR SEGMENT: RIEGER'S ANOMALY.
Topics: Anterior Chamber; Anterior Eye Segment; Congenital Abnormalities; Cornea; Eye Abnormalities; Eye Dis | 1965 |
[Irido-corneal dysgenesis, Axenfeld Rieger syndrome].
Topics: Abnormalities, Multiple; Adult; Anterior Eye Segment; Corneal Opacity; Diagnosis, Differential; Eye | 2007 |
Plateau iris syndrome in a child.
Topics: Child; Eye Diseases, Hereditary; Glaucoma, Angle-Closure; Humans; Iridectomy; Iris; Male; Microscopy | 2008 |
[Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].
Topics: Abnormalities, Multiple; Adult; Cornea; Craniofacial Abnormalities; Diagnostic Techniques, Ophthalmo | 2007 |
Clinical manifestation of a novel PAX6 mutation Arg128Pro.
Topics: Adult; Aged; Arginine; Cataract; Corneal Opacity; Eye Diseases, Hereditary; Eye Proteins; Female; Fo | 2008 |
Primary congenital ectropion uveae associated with vitreoretinal degeneration.
Topics: Adolescent; Dark Adaptation; Ectropion; Electrooculography; Electroretinography; Eye Diseases, Hered | 1998 |
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice.
Topics: Aging; Animals; Anterior Eye Segment; Atrophy; Cell Death; Disease Models, Animal; Disease Progressi | 1998 |
Ectopia lentis et pupillae. A hypothesis revisited.
Topics: Anterior Eye Segment; Cataract Extraction; Ectopia Lentis; Eye Diseases, Hereditary; Female; Humans; | 1998 |
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations.
Topics: Anterior Eye Segment; DNA Mutational Analysis; Eye Diseases, Hereditary; Eye Proteins; Female; Heter | 2000 |
Hereditary optic pit and iris coloboma in three generations of a single family.
Topics: Coloboma; Eye Diseases, Hereditary; Female; Humans; Iris; Laser Coagulation; Male; Middle Aged; Opti | 2001 |
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 |