Patterned Dystrophy of Retinal Pigment Epithelium
General: Autosomal dominant; probably there is a migration of pigment granules in the pigment epithelium, resulting in a specific conuration.
Ocular: Reticular fishnet-like dystrophy; macroreticular (spider shaped); butterfly-shaped pigment dystrophy of fovea.
Clinical: None.
Deutman AF. Macular dystrophies. In: Ryan SJ. ed. Retina, vol. II, 2nd ed. St. Louis: Mosby, 1994.
Hsieh RC, et al. Patterned dystrophies of retinal pigment epithelium. Arch Ophthalmol 1977; 95:429-435.
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/.
O'Donnel FE, et al. Autosomal dominant dystrophy of the retinal pigment epithelium. Arch Ophthalmol 1979; 97:680.
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