Autosomal dominant optic atrophy, classic form

One of the most common forms of hereditary optic neuropathy characterized by progressive bilateral visual loss during the first decade of life, associated with optic disk pallor, visual field and color vision defects.

Also known as: Kjer optic atrophy, autosomal dominant optic atrophy, Kjer type, optic atrophy type 1, Kjer-type optic atrophy, OAK, OPA1, optic atrophy 1, optic atrophy, Kjer type

20 clinical trials for this condition and its sub-types.