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