2-propanol has been researched along with Abnormalities, Teeth in 26 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "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) |
| "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) |
| "The Rieger syndrome is a rare, autosomal dominant disorder." | 1.27 | Oral manifestations of the Rieger syndrome: report of case. ( Drum, MA; Guckes, AD; Kaiser-Kupfer, MI; Roberts, MW, 1985) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 12 (46.15) | 18.7374 |
| 1990's | 3 (11.54) | 18.2507 |
| 2000's | 9 (34.62) | 29.6817 |
| 2010's | 2 (7.69) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Masket, S | 1 |
| Riise, R | 2 |
| D'haene, B | 1 |
| De Baere, E | 1 |
| Grønskov, K | 1 |
| Brøndum-Nielsen, K | 2 |
| Sobreira, N | 1 |
| Walsh, MF | 1 |
| Batista, D | 1 |
| Wang, T | 1 |
| Tallón-Walton, V | 1 |
| Nieminen, P | 1 |
| Arte, S | 1 |
| Ustrell-Torrent, JM | 1 |
| Carvalho-Lobato, P | 1 |
| Manzanares-Céspedes, MC | 1 |
| Vieira, H | 1 |
| Gregory-Evans, K | 1 |
| Lim, N | 1 |
| Brookes, JL | 1 |
| Brueton, LA | 1 |
| Gregory-Evans, CY | 1 |
| Honkanen, RA | 1 |
| Nishimura, DY | 1 |
| Swiderski, RE | 1 |
| Bennett, SR | 1 |
| Hong, S | 1 |
| Kwon, YH | 1 |
| Stone, EM | 1 |
| Sheffield, VC | 1 |
| Alward, WL | 1 |
| REJCHRT, B | 1 |
| MIKSA, J | 1 |
| LEMMINGSON, W | 1 |
| RIETHE, P | 1 |
| Singh, J | 1 |
| Pannu, K | 1 |
| Lehl, G | 1 |
| Meyer, CH | 1 |
| Rodrigues, EB | 1 |
| Mennel, S | 1 |
| Strempel, I | 1 |
| Dressler, P | 1 |
| Gramer, E | 1 |
| Ito, YA | 1 |
| Footz, TK | 1 |
| Murphy, TC | 1 |
| Courtens, W | 1 |
| Walter, MA | 2 |
| Binder, K | 1 |
| Müller-Jensen, K | 1 |
| Mirzayans, F | 1 |
| Mears, AJ | 1 |
| Hickey, K | 1 |
| Pearce, WG | 1 |
| Gündüz, K | 1 |
| Günalp, I | 1 |
| Erden, I | 1 |
| Storhaug, K | 1 |
| Cross, HE | 1 |
| Gorlin, RJ | 2 |
| Cervenka, J | 1 |
| Moller, K | 1 |
| Horrobin, M | 1 |
| Witkop, CJ | 1 |
| Jones, KL | 1 |
| Smith, DW | 1 |
| Harvey, MA | 1 |
| Hall, BD | 1 |
| Quan, L | 1 |
| Holmström, GE | 1 |
| Reardon, WP | 1 |
| Baraitser, M | 1 |
| Elston, JS | 1 |
| Taylor, DS | 1 |
| Sachdev, MS | 1 |
| Sood, NN | 1 |
| Kumar, H | 1 |
| Ghose, S | 1 |
| Drum, MA | 1 |
| Kaiser-Kupfer, MI | 1 |
| Guckes, AD | 1 |
| Roberts, MW | 1 |
| Schäfer, WD | 1 |
| Schell-Wölker, H | 1 |
| Henkes, HE | 1 |
| Sedano, HO | 1 |
| Feingold, M | 1 |
| Shiere, F | 1 |
| Fogels, HR | 1 |
| Donaldson, D | 1 |
3 reviews available for 2-propanol and Abnormalities, Teeth
| Article | Year |
|---|---|
Oral findings in Midline Syndrome: a case report and literature review.
Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Child; Cleft Palate; Coloboma; Encephalocele; | 2010 |
Penetrance and variability in anterior chamber malformations.
Topics: Anterior Chamber; Chromosomes, Human, 13-15; Chromosomes, Human, 16-18; Corneal Opacity; Descemet Me | 1979 |
Oral manifestations of systemic genetic disorders. 3.
Topics: Abnormalities, Multiple; Anodontia; Central Nervous System Diseases; Cornea; Ectodermal Dysplasia; E | 1971 |
23 other studies available for 2-propanol and Abnormalities, Teeth
| Article | Year |
|---|---|
Cataract surgical problem: February consultation #1.
Topics: Cataract; Cataract Extraction; Coloboma; Cornea; Craniofacial Abnormalities; Eye Abnormalities; Foot | 2014 |
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 |
Interstitial deletion 5q14.3-q21 associated with iris coloboma, hearing loss, dental anomaly, moderate intellectual disability, and attention deficit and hyperactivity disorder.
Topics: Attention Deficit Disorder with Hyperactivity; Child; Chromosome Deletion; Chromosomes, Human, Pair | 2009 |
First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
Topics: Adult; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 20; Coloboma; DNA Mutational A | 2002 |
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 |
Mesodermal dysgenesis of the cornea and iris.
Topics: Cornea; Humans; Iris; Iris Diseases; Tooth Abnormalities | 1952 |
[Observations on mesodermal dysgenesis of the cornea & iris associated with oligodontia].
Topics: Cornea; Eye Abnormalities; Humans; Iris; Tooth Abnormalities | 1958 |
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 |
[Juvenile glaucoma, cataract and tooth abnormalities in a young patient].
Topics: Abnormalities, Multiple; Adult; Cataract; Cataract Extraction; Cornea; Glaucoma; Humans; Iris; Male; | 2005 |
[Morphology, family history, and age at diagnosis of 26 patients with Axenfeld-Rieger syndrome and glaucoma or ocular hypertension].
Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosomes, Human, Pair 13; Diagnosis, Differentia | 2006 |
Analyses of a novel L130F missense mutation in FOXC1.
Topics: Abnormalities, Multiple; Adult; Animals; Anterior Eye Segment; Cell Culture Techniques; Chlorocebus | 2007 |
[Anterior cleavage syndrome associated with endocrine orbitopathy (author's transl)].
Topics: Adult; Corneal Dystrophies, Hereditary; Female; Glaucoma; Graves Disease; Humans; Iris; Syndrome; To | 1981 |
Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.
Topics: Abnormalities, Multiple; Adult; Anterior Eye Segment; Chromosome Mapping; Chromosomes, Human, Pair 4 | 1996 |
Focal dermal hypoplasia (Goltz's syndrome).
Topics: Abnormalities, Multiple; Adolescent; Brain; Choroid; Coloboma; Cornea; Eye Abnormalities; Female; Fo | 1997 |
Rieger syndrome is associated with PAX6 deletion.
Topics: Abnormalities, Multiple; Anterior Eye Segment; Child; Chromosomes, Human, Pair 6; Eye Abnormalities; | 2001 |
Malformation syndromes. A selected miscellany.
Topics: Abnormalities, Multiple; Adolescent; Child; Child, Preschool; Chromosomes, Human, 6-12 and X; Dental | 1975 |
Older paternal age and fresh gene mutation: data on additional disorders.
Topics: Age Factors; Bone Cysts; Brain Diseases; Carcinoma, Basal Cell; Cleidocranial Dysplasia; Congenital | 1975 |
Heterogeneity in dominant anterior segment malformations.
Topics: Abnormalities, Multiple; Adult; Anterior Eye Segment; Child; Cornea; Eye Diseases; Female; Genes, Do | 1991 |
Bilateral aniridia with Marfan's syndrome and dental anomalies--a new association.
Topics: Adolescent; Eye; Female; Hand; Humans; Iris; Marfan Syndrome; Radiography, Dental; Radiography, Thor | 1986 |
Oral manifestations of the Rieger syndrome: report of case.
Topics: Adult; Anodontia; Anterior Eye Segment; Female; Fluorosis, Dental; Humans; Infant; Iris; Male; Pedig | 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 |
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 |
Rieger's syndrome.
Topics: Abnormalities, Multiple; Adult; Child; Dental Enamel Hypoplasia; Eye Diseases; Glaucoma; Growth Horm | 1969 |