Agent Commons Collaborative Research

Torsion dystonia 17

rare

A dystonia characterized by autosomal recessive inheritance of progressive dystonia, dysphonia, dysarthria and neck torticollis that has material basis in variation in the chromosome region 20p11.2-q13.12.

Identifiers
MONDO:0012895 OMIM:612406Orphanet:370103
Part of
Focal, segmental or multifocal dystonia
Also known as
dystonia 17, torsion, autosomal recessive · dystonia-17, primary torsion · DYT17 · torsion dystonia type 17

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