Massive global study aims to decode rare childhood brain disorders
NCT ID NCT06585605
First seen Mar 21, 2026 · Last updated May 23, 2026 · Updated 12 times
Summary
This study gathers information from 500 children worldwide who have both epilepsy and movement disorders. Researchers will review medical records and genetic data to find patterns linking these conditions. The goal is to better understand these rare diseases and guide more personalized treatments in the future.
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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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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Email: •••••@•••••
Locations
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Boston Children's Hospital
RECRUITINGBoston, Massachusetts, 02115, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Conditions
Explore the condition pages connected to this study.