Retinoschisis (RS)
General: Sex-linked; may not manifest until middle life.
Ocular: Intraretinal splitting due to degeneration or detachment of retina; retinal atrophy with sclerosis of the choroid; cystic maculopathy.
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/.
Wieacker P, et al. Linkage relationships between retinoschisis Xg and a cloned DNA sequence from the distal short arm of X chromosome. Hum Genet 1983; 64:143-l45.
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