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:329466
dystonia 25
OrphanetORPHA:329466
Treatments0 drug(s)
Symptoms on record7 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO