Tiny brain study seeks to unlock secrets of rare movement disorder
NCT ID NCT06701851
First seen Apr 29, 2026 · Last updated Jun 09, 2026 · Updated 9 times
Summary
This study looks at brain activity during sudden movement episodes in people with a rare genetic condition called PRRT2-related paroxysmal dyskinesia. Only one participant who can control these episodes will be enrolled. Using MRI and EEG, researchers hope to understand which brain areas are involved, especially the striatum and cerebellum.
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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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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Institut du Cerveau de la Moelle Epinière ICM, Hôpital Pitié Salpêtrière,
RECRUITINGParis, 75651 PARIS cedex 13, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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