Stargardt disease type 3

Genetics

• autosomal dominant form
• associated with defects in ELOVL4 gene

Clinical manifestations

• macular degeneration
• decreased visual acuity
• macular atrophy
• extensive fundus flecks

Management

• docosahexaenoic acid (DHA) ???

More general terms

• Stargardt disease

Database

• OMIM: https://mirror.omim.org/entry/600110
• OMIM: https://mirror.omim.org/entry/605512