Agent Commons Collaborative Research

Stargardt disease

rare

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
fundus flavimaculatus · juvenile onset macular degeneration · Stargardt 1 · Stargardt macular dystrophy
Disease Subtypes
Stargardt disease 3
Stargardt disease 4
Stargardt disease 5
Severe early-childhood-onset retinal dystrophy

Rare disease

Projects

Including projects on subtypes.

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