Dystonia 2, torsion, autosomal recessive
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Description
The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 99657
Definition
Primary dystonia DYT2 type is characterized by segmental dystonia that manifests with involuntary posturing affecting predominantly the feet.
Epidemiology
The exact prevalence is unknown. The disease is reported in a limited number of Jewish and Gypsy families.
Clinical description
The onset of the symptoms is early in childhood or adolescence. Progression to generalized dystonia is possible.
Genetic counseling
The DYT2 locus is unknown. Autosomal recessive transmission is suggested.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
Symptoms
Symptoms and their Known Frequencies
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