dystonia 21
ORPHA: 306734
Overview
dystonia characterized by autosomal dominant inheritance of late onset pure torsion dystonia that has material basis in variation in the chromosome region 2q14.3-q21.3
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with dystonia 21, sourced from HPO and Orphanet clinical annotations.
DystoniaTorticollisBlepharospasmParoxysmal dystoniaFocal dystoniaGeneralized dystoniaLimb dystoniaAxial dystoniaLaryngeal dystonia
Classification & Codes
Orphanet Code
ORPHA:306734dystonia 21
| Orphanet | ORPHA:306734 |
| Treatments | 0 drug(s) |
| Symptoms on record | 9 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO