Optic Atrophy, Autosomal Dominant

Synonyms

Atrophies, Juvenile Optic

Atrophies, Kjer-Type Optic

Atrophy, Juvenile Optic

Atrophy, Kjer's Optic

Atrophy, Kjer-Type Optic

Autosomal Dominant Optic Atrophy

Autosomal Dominant Optic Atrophy Kjer Type

Dominant Optic Atrophies

Dominant Optic Atrophy

Juvenile Optic Atrophies

Juvenile Optic Atrophy

Kjer Optic Atrophy

Kjer Type Optic Atrophy

Kjer's Optic Atrophy

Kjer-Type Optic Atrophies

Kjer-Type Optic Atrophy

Kjers Optic Atrophy

Optic Atrophies, Dominant

Optic Atrophies, Juvenile

Optic Atrophies, Kjer-Type

Optic Atrophy 1

Optic Atrophy 1s

Optic Atrophy Type 1

Optic Atrophy, Dominant

Optic Atrophy, Hereditary, Autosomal Dominant

Optic Atrophy, Juvenile

Optic Atrophy, Kjer Type

Optic Atrophy, Kjer's

Optic Atrophy, Kjer-Type

Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.