New study aims to map social challenges in rare genetic disorder
NCT ID NCT07469566
First seen Mar 22, 2026 · Last updated May 07, 2026 · Updated 7 times
Summary
This study follows 15 people with 7q11.23 microduplication syndrome (7DUP) from age 5 to 50 to track how social skills develop over time. Researchers will use interviews, questionnaires, and tests to measure social, communication, and motor milestones. The goal is to better understand the condition and identify the best ways to measure improvement in future treatment trials.
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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: •••••@•••••
Locations
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Developmental Anomalies Reference Center, Genetics Department Woman Mother and Child Hospital, University Hospital of Lyon, Hospices Civils de Lyon
Bron, 69677, France
Contact
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Reference Center of Rare Disease with Intellectual Disability- in Lyon, Woman Mother and Child Hospital, University Hospital of Lyon, Hospices Civils de Lyon
Bron, 69677, France
Contact
Conditions
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