Scientists track rare dystonia to map its genetic roots

NCT ID NCT00682513

Ongoing Knowledge-focused Sponsor: State University of New York at Buffalo Source: ClinicalTrials.gov ↗

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study is observing up to 198 people with rapid-onset dystonia-parkinsonism (RDP) or related genetic mutations. Researchers aim to identify affected individuals, document how common the disease is, and track its progression over time. Participants undergo assessments of symptom severity and neuropsychiatric health, but no treatment is being tested.

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Conditions

The condition(s) this trial relates to.

alternating hemiplegia of childhood Dystonia dystonia 12 dystonic disorder parkinsonian disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

DYSTONIA PARKINSONISM

Contacts and locations

Locations

University at Buffalo

Buffalo, New York, 14203, United States
University of Miami

Miami, Florida, 33136, United States

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