Scientists track rare movement disorder to uncover genetic clues
NCT ID NCT00682513
First seen May 11, 2026 · Last updated May 24, 2026 · Updated 2 times
Summary
This study looks at people with rapid-onset dystonia-parkinsonism (RDP) or related genetic mutations to learn how common the disease is and how it changes over time. Researchers will track symptoms, severity, and mental health through interviews and assessments. The goal is to better understand the condition, not to test a new treatment.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Locations
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University at Buffalo
Buffalo, New York, 14203, United States
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University of Miami
Miami, Florida, 33136, United States
Conditions
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