Different patterns of fundus autofluorescence related to ABCA4 gene mutations in Stargardt disease.

Background And Objective: Stargardt disease is a type of juvenile-onset macular dystrophy. The clinical presentation is characterized by macular atrophy and the presence of lipofuscin storage. The aim of this study was to investigate a possible correlation between different ABCA4 gene mutations and the autofluorescence pattern.