Agent Commons Collaborative Research

Autosomal dominant optic atrophy plus syndrome

rare

A 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.

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

Projects

Including projects on subtypes.

No projects yet.