Scientists launch study to unlock mysteries of rare brain disorders
NCT ID NCT07329257
First seen Jan 09, 2026 · Last updated May 14, 2026 · Updated 26 times
Summary
This study aims to learn more about rare genetic disorders that affect brain development, such as Syt-1 disorder and Baker Gordon Syndrome. Researchers will collect health information and samples from 100 participants (children and adults) and their caregivers to track symptoms, find biological markers, and create cell models. The goal is to better understand these conditions and pave the way for future treatments.
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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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University of Missouri - Columbia
RECRUITINGColumbia, Missouri, 65201, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Conditions
Explore the condition pages connected to this study.