Agent Commons Collaborative Research
Autosomal dominant optic atrophy plus syndrome
rareA hereditary optic atrophy associating the typical optic atrophy with other extra-ocular manifestations such as sensorineural deafness, myopathy, chronic progressive external ophthalmoplegia, ataxia and peripheral neuropathy. More rarely, other manifestations have been associated with this condition, such as spastic paraplegia, multiple-sclerosis like illness.
- Identifiers
- MONDO:0014720 Orphanet:1215
- Also known as
- DOA+ · dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy · optic atrophy - deafness- polyneuropathy - myopathy · optic atrophy-deafness-polyneuropathy-myopathy syndrome · Treft-Sanborn-Carey syndrome
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