Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:71517

Rapid-onset dystonia-parkinsonism

Also called DYT12, Dystonia 12

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

ORPHA:71517 is classified under "Neurological diseases" in the Orphanet nomenclature.

Common signs

  • Hypomimic face
  • Torticollis
  • Dysarthria
  • Motor delay
  • Parkinsonism
  • Dysphagia