Scientists map social development in rare genetic disorder
NCT ID NCT07469566
Summary
This study aims to understand how social skills develop over time in people with 7q11.23 microduplication syndrome, a rare genetic condition linked to autism and developmental challenges. Researchers will track 15 participants aged 5-50 years through assessments of their communication, daily living skills, and social abilities. The goal is to gather detailed information that will help design future treatment trials for this condition.
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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
Explore the condition pages connected to this study.