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Deafness dystonia syndrome

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Description

Males with deafness-dystonia-optic neuronopathy (DDON) syndrome have prelingual or postlingual sensorineural hearing impairment in early childhood, slowly progressive dystonia or ataxia in the teens, slowly progressive decreased visual acuity from optic atrophy beginning at approximately age 20 years, and dementia beginning at approximately age 40 years. Psychiatric symptoms such as personality change and paranoia may appear in childhood and progress. The hearing impairment appears to be consistent in age of onset and progression, whereas the neurologic, visual, and neuropsychiatric signs vary in degree of severity and rate of progression. Females may have mild hearing impairment and focal dystonia.

GeneReviews

  • Mode of Inheritance

  • X-linked recessive inheritance

VARIANTS

6

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Genes

External Links

  • OMIM

    304700

  • Orphanet

    52368

  • HPO
  • Medgen

    C0796074

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