Foveal Hypoplasia and Presenile Cataract Syndrome (O'Donnell-Pappas Syndrome) 4
General: Autosomal dominant.
Ocular: Foveal hypoplasia; nystagmus; presenil 343i83d e cataract; peripheral corneal pannus.
Clinical: None.
O'Donnell FE, Pappas HR. Autosomal dominant foveal hypoplasia and presenile cataracts: a new syndrome. Arch Ophthalmol 1982; 100:279-281.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.
Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.
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