31 / 37
Inherited Disease
29
af
Diagnostic Atlas
A Retinal Reference Guide
Stargardt’s Disease
is a hereditary condition of degeneration in the macula
characterized by central vision loss with minimal changes
visible with an ophthamoscope. In advanced disease, the
macula may show pigment clumping surrounded by a
hammered-metal appearance. It is often associated with
fundus flavimaculatus.