New study aims to unlock mysteries of rare genetic disorder
NCT ID NCT06399952
First seen Jun 11, 2026 · Last updated Jun 16, 2026 · Updated 2 times
Summary
This study follows 50 children and adults with Baker Gordon Syndrome, a rare genetic condition causing developmental delays, autism traits, and seizures. Researchers will collect medical history and track symptoms over time to better understand the disease. The goal is to create tools that help doctors measure the condition, paving 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: •••••@•••••
Conditions
Explore the condition pages connected to this study.