Snowflake Vitreoretinal Degeneration 1 1
General: Autosomal dominant; very small yellow-w 313b19d hite dots on the retina.
Ocular: Fibrillar vitreous degeneration; thickening of cortical vitreous; optically empty vitreous cavity; vitreous hemorrhage; posterior vitreous detachment with collapse; retinal detachment; retinal hemorrhage; retinal holes; marked retinal pigmentation; obliterated retinal vessels; sheathed retinal vessels; preretinal retraction; chorioretinal atrophy; corneal opacities; myopia; hyperopia; astigmatism; amblyopia; cataract; glaucoma.
Clinical: None.
Gheiler M, et al. Hereditary snowflake vitreoretinal degeneration. Birth Defects 1982; 18:577-580.
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/.
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