Peters Anomaly
What's New
Last Posted: Mar 05, 2023
- Identification of PITX3 mutations in individuals with various ocular developmental defects.
Zazo Seco Celia, et al. Ophthalmic genetics 2018 0 (3) 314-320 - Dominant variants in PRR12 result in unilateral or bilateral complex microphthalmia.
Reis Linda M, et al. Clinical genetics 2020 0 (3) 437-442 - Identification of OAF and PVRL1 as candidate genes for an ocular anomaly characterized by Peters anomaly type 2 and ectopia lentis.
David Dezs?, et al. Experimental eye research 2018 0 161-170 - Molecular basis of Peters anomaly in Saudi Arabia.
Edward Deepak, et al. Ophthalmic genetics 2004 0 (4) 257-70 - First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients.
Chesneau Bertrand, et al. Clinical genetics 2022 0 (5-6) 494-506 - Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.
Reis Linda M, et al. Molecular vision 2016 0 1229-1238 - Whole exome sequence analysis of Peters anomaly.
Weh Eric, et al. Human genetics 2014 12 (12) 1497-511 - CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited.
Kelberman Daniel, et al. Ophthalmology 2011 9 (9) 1865-73 - Peters anomaly
From NCATS Genetic and Rare Diseases Information Center - Mutation spectrum of the CYP1B1 gene for congenital glaucoma in the Japanese population.
Fuse Nobuo, et al. Japanese journal of ophthalmology 2010 1 (1) 1-6
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- Page last reviewed:Feb 1, 2024
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