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Stargardt Disease (Stargardt Macular Dystrophy, Fundus Flavimaculatus)

Stargardt Disease (Stargardt Macular Dystrophy, Fundus Flavimaculatus)

Stargardt Disease (Stargardt Macular Dystrophy, Fundus Flavimaculatus)

-Polymorphic sheen in the macula which is generally ovoid in appearance,surrounding the fovea.
-F.A:* in the early stages of the disease will show a so-called “dark choroid” corresponding to the paramacular region and peripheral fundus, where there is accumulation of lipofuscin in the pigment epithelium which blocks choroidal fluorescence.
*A hyperfluorescence is seen where there is atrophy of the pigment epithelium.
-Some patients with Stargardt disease demonstrate flecks in the paramacular region, along the arcades and in the near peripheral fundus.
-Most common hereditary macular dystrophy. It is characterized by bilateral atrophy of the macula and underlying RPE, central vision impairment.

Stargardt Disease (Stargardt Macular Dystrophy, Fundus Flavimaculatus)

Stargardt Disease (Stargardt Macular Dystrophy, Fundus Flavimaculatus)

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Ophthalmology Atlas(Photos of cases)

Stargardt Disease (Stargardt Macular Dystrophy, Fundus Flavimaculatus)

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Stargardt Disease (Stargardt Macular Dystrophy, Fundus Flavimaculatus) -Polymorphic sheen in the macula which is generally ovoid in appearance,surrounding the fovea. -F.A:* in the early stages of the disease will show a so-called “dark choroid” corresponding to the paramacular region and peripheral fundus, where there is accumulation of lipofuscin in the pigment epithelium which blocks choroidal …

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