Global hunt for answers to mysterious childhood brain disorders
NCT ID NCT06585605
Summary
This study aims to better understand rare genetic disorders that cause both epilepsy and movement problems in children. Researchers will collect medical information from 500 children worldwide who have specific genetic changes and these symptoms. By analyzing this data, they hope to identify patterns that could lead to better diagnosis and future treatments for these complex conditions.
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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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Email: •••••@•••••
Locations
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Boston Children's Hospital
RECRUITINGBoston, Massachusetts, 02115, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Conditions
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