Macular Dystrophy, Fenestrated Sheen Type
General: Autosomal dominant; progressive; onset in the sixth decade.
Ocular: Yellowish retractile sheen in sensory retina at the macula; red fenestrations present within sheen; hypopigmentation of retinal pigment epithelium.
Clinical: None.
Fishman GA, et al. Dominantly inherited cystoid macular edema. Ann Ophthalmol 1979; 11:21-27.
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/.
Sneed SR, Sieving PA. Fenestrated sheen macular dystrophy. Am J Ophthalmol 1991; 112:1.
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