Clinical Features of a Stargardt-Like Dominant Progressive Macular Dystrophy With Genetic Linkage to Chromosome 6q

Abstract excerpt

BACKGROUND AND OBJECTIVE: We identified a large family affected with a macular dystrophy whose main clinical features are similar to those of Stargardt's disease. Unlike true Stargardt's disease, the disorder in this family is inherited in an autosomal dominant fashion. We sought to identify the chromosomal location of the disease-causing gene and to clinically define the phenotype in a number of affected family...

Topics

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

• Share to Photoreceptor and optogenetics research
• Share to Retinal Development and Disorders
• Share to Retinal Diseases and Treatments