Unusual clinical phenotype of Stargardt disease.

Abstract excerpt

Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phenotypes have also been associated with mutations in this gene. We describe an observational case report of an unusual clinical phenotype of Stargardt disease. The ophthalmological examination included best corrected visual acuity, color and autofluorescence photography, fluorescein angiography, optical coherence...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Stargardt Disease
• Share to ATP-Binding Cassette Transporters