dystonia 25
ORPHA: 329466
Overview
multifocal dystonia characterized by autosomal dominant inheritance of cervical, laryngeal and hand-forearm dystonia that has material basis in heterozygous mutation in the GNAL gene on chromosome 18p11
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 25, sourced from HPO and Orphanet clinical annotations.
Focal dystoniaTorticollisLimb dystoniaAxial dystoniaLaryngeal dystoniaCraniofacial dystoniaLingual dystonia
Classification & Codes
Orphanet Code
ORPHA:329466dystonia 25
| Orphanet | ORPHA:329466 |
| Treatments | 0 drug(s) |
| Symptoms on record | 7 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO