Stargardt research hub

An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 Gene

This study looks closely at how Stargardt Disease type 1 (STGD1) changes over time. Researchers want to understand the disease better by watching people who have it. This will help them design better studies in the future to test new treatments for Stargardt.