Conditions / Genetic
Stargardt disease 3
info · Genetic
A stargardt disease that is characterized by macular pigmentary changes and yellow flecks and macular retinal pigment epithelium defects and has_material_basis_in heterozygous mutation in the ELOVL4 gene on chromosome 6q14.
Signs and symptoms
- Macular flecks
- Reduced visual acuity
- Visual impairment
- Macular atrophy
- Macular dystrophy