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Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy

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Description

Syndromic optic atrophy, also known as DOA+ syndrome, is a neurologic disorder characterized most commonly by an insidious onset of visual loss and sensorineural hearing loss in childhood with variable presentation of other clinical manifestations including progressive external ophthalmoplegia (PEO), muscle cramps, hyperreflexia, and ataxia. There appears to be a wide range of intermediate phenotypes (Yu-Wai-Man et al., 2010).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

18

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Genes

External Links

  • OMIM

    125250

  • Orphanet

    3212

  • HPO
  • Medgen

    C3276549

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