First-Ever study to map brain and language challenges in rare MYT1L syndrome
NCT ID NCT07008612
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aims to describe the language, thinking, and behavior patterns in people with MYT1L syndrome, a rare genetic condition that affects development. Researchers will work with 50 French-speaking participants aged 6 and older, using interviews and tests to build a detailed profile. The goal is to better understand the condition, not to test a treatment.
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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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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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University Hospital of Rouen
RECRUITINGRouen, 76031, France
Contact Phone: •••-•••-•••• Email: •••••@•••••