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

60 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by