Retinal Detachment
General: Autosomal dominant; multilayered retinal tissue sepa 121b17b rates along an interface formed in course of embryonic development.
Ocular: Retinal tear or hole; retinal detachment.
Clinical: None.
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/.
McNeil NA, McPherson A. The inheritance of detached retina in a texas family. J Hered 1971; 62:73-76.
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