Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:314404

Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome

Also called ADCA-DN syndrome, Autosomal dominant cerebellar ataxia-hearing loss-narcolepsy syndrome

Body system
Neurological diseases
Inheritance pattern
Autosomal dominant, Not applicable
Typical age of onset
Adult
Estimated prevalence
<1 / 1 000 000 (Worldwide)
Rarity class
<1 / 1 000 000

ORPHA:314404 is classified under "Neurological diseases" in the Orphanet nomenclature.

Common signs

  • Sensorineural hearing impairment
  • Narcolepsy
  • Optic atrophy
  • Abnormality of mitochondrial metabolism
  • Urinary incontinence
  • Cataract