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Stargardt disease | Ricardo Leitão Guerra, MD

59yo

Stargardt disease, associated with mutations in the ABCA4 gene, is the most common form of inherited juvenile macular degeneration. It is characterized by progressive loss of central vision, often beginning in childhood or adolescence. The disease leads to the accumulation of lipofuscin in the retinal pigment epithelium, visible as yellowish flecks on imaging studies, predominantly affecting the macula and central vision.

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