Scientists track rare movement disorder to uncover genetic clues
NCT ID NCT00682513
First seen May 11, 2026 · Last updated May 16, 2026 · Updated 1 time
Summary
This study looks at people with rapid-onset dystonia-parkinsonism (RDP), a rare movement disorder. Researchers aim to find genetic mutations linked to the disease and document how symptoms develop and change over time. About 200 participants are involved, and the focus is on observation and measurement, not testing 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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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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