Stargardt disease

MONDO:0019353

Stargardt disease, also known as Stargardt 1 (STGD1), is an autosomal recessive form of retinal dystrophy that is usually characterized by a progressive loss of central vision associated with irregular macular and perimacular yellow-white fundus flecks, and a so-called ''beaten bronze'' atrophic central macular lesion.

Also known as: Stargardt 1, fundus flavimaculatus, Stargardt disease 1, Stargardt macular dystrophy, juvenile onset macular degeneration

57 clinical trials for this condition and its sub-types, 35 tagged with Stargardt disease itself.

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