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autosomal dominant optic atrophy plus syndrome

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Autosomal dominant optic atrophy plus syndrome (ADOA plus) is a variant of autosomal dominant optic atrophy (ADOA) 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.

Synonyms

  • DOA+
  • Treft-Sanborn-Carey syndrome
  • dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy
  • optic atrophy - deafness- polyneuropathy - myopathy
  • optic atrophy type 8
  • optic atrophy-deafness-polyneuropathy-myopathy syndromeDOA+
  • Treft-Sanborn-Carey syndrome
  • dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy
  • optic atrophy - deafness- polyneuropathy - myopathy
  • optic atrophy type 8
  • optic atrophy-deafness-polyneuropathy-myopathy syndrome
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