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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) ???
Interactions
disease interactions
General
Stargardt disease
Database Correlations
OMIM correlations
MORBIDMAP 605512