Stargardt disease 3
A hereditary form of macular degeration. Affected individuals may experience central vision loss as children or young adults and some may also have macular flecks. Mutations have been identified in the ELOVL4 gene. OMIM: 600110
Also Known As:
Macular dystrophy with flecks, type 3; Macular dystrophy, autosomal dominant, chromosome 6-linked,; Stargardt-Like Macular Dystrophy, Autosomal Dominant
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