Dystonia 12

Common Name(s)

Dystonia 12

Dystonia-12, also known as rapid-onset dystonia-parkinsonism, is an autosomal dominant disorder characterized by abrupt onset of asymmetric dystonia and parkinsonism in young adulthood, often after a trigger such as physical overexertion, trauma, heat, or fever. Affected individuals also show slowly progressive nonparoxysmal neurologic deterioration in a rostrocaudal gradient with prominent bulbar dysfunction (summary by {11:Rosewich et al., 2014}).
 

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Condition Specific Organizations

Following organizations serve the condition "Dystonia 12" for support, advocacy or research.

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Scientific Literature

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Identification, Prevalence, and Lifespan of Rapid-Onset Dystonia-Parkinsonism
 

Status: Recruiting

Condition Summary: Dystonia; Parkinsonism

 

Last Updated: 26 May 2011

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