Conditions / Genetic
optic atrophy 6
info · Genetic
An optic atrophy characterized by early onset of slowly progressive isolated optic atrophy that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 8q21-q22.
Signs and symptoms
- Photophobia
- Visual impairment
- Optic atrophy
- Red-green dyschromatopsia
- Nystagmus
- Retinal degeneration
Also known as: OPA6