Vitreoretinochoroidopathy (VRCP; Autosomal Dominant Vitreoretinochoroidopathy; ADVIRC) 1
General: Autosomal dominant.
Ocular: Chorioretinal hypopigmentation or hyperpigmentation; preretinal punctate opacities; retinal arteriolar narrowing and occlusion; choroidal atrophy; diffuse retinal vascular incompetence; cystoid macular edema; presenile cataracts; fibrillar condensation and moderate pleocytosis of vitreous; myopia; optically empty vitreous; lattice degeneration; retinal breaks; retinal detachment; glaucoma; spontaneous vitreous hemorrhage.
Clinical: None.
Blair NP, et al. Autosomal dominant vitreoretinochoroidopathy. Br J Ophthalmol 1984; 68:2-9.
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/.
Traboulsi EL, Payne JW. Autosomal dominant vitreoretinopathy: report of the third family. Arch Ophthalmol 1993; 111:194-l96.
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