Phenotypic Spectrum of Peters Anomaly: Implications for Management
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology
Reference30 articles.
1. Ueber angeborene Decectbildung der Descemetschen membran [in German];Peters;Klin Monbl Augenheilkd,1906
2. A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly;Doucette;Eur J Hum Genet,2011
3. Chromosome abnormalities and the genetics of congenital corneal opacification;Mataftsi;Mol Vis,2011
4. Congenital corneal leukomas. 3. Histopathologic findings in 13 eyes with noncentral defect in Descemet's membrane;Townsend;Am J Ophthalmol,1974
5. Corneal transplantation in children with Peters anomaly and mesenchymal dysgenesis. Multicenter Pediatric Keratoplasty Study;Dana;Ophthalmology,1997
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2. Peters anomaly: An overview;Taiwan Journal of Ophthalmology;2023
3. Genetics of the anterior segment dysgenesis;Taiwan Journal of Ophthalmology;2023
4. Peters Anomaly with Glaucoma;Childhood Glaucoma;2023
5. A 17-year stepped surgical treatment of Peters anomaly in a child;Pacific Medical Journal;2022-09-08
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