Primary dystonia, DYT6 type
Synonyms: DYT6 | Generalized cervical and upper-limb-onset dystonia | Idiopathic torsion dystonia of mixed type
A rare genetic movement disorder characterized by dystonia affecting at first an upper limb less frequently beginning in the head and neck region before slowly spreading to other locations. The clinical spectrum like age of onset is variable with focal segmental or generalized distribution but cranial involvement with speech difficulties and cervical involvement are typical whereas lower limbs are often spared. With progression of the disease many patients suffer from generalized dystonia while mostly remaining ambulatory.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version December 2023
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Primary dystonia, DYT6 type?
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Advocacy Organizations
COMBINEDBrain Inc
COMBINEDBrain is a consortium for outcome measures and biomarkers for neurodevelopmental disorders. We are collaborating to cure rare, non-verbal brain disorders.
Moonshots for Unicorns
Curing single-gene disorders
Project CASK
To fund research for treatment and/or a cure for CASK Gene Disorder
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.