New study aims to map social challenges in rare genetic syndrome

NCT ID NCT07469566

Recruiting now Knowledge-focused Sponsor: Hospices Civils de Lyon Source: ClinicalTrials.gov ↗

First seen Jun 24, 2026 · Last updated Aug 04, 2026 · Updated 3 times

Summary

This study will follow 15 people aged 5 to 50 with 7q11.23 microduplication syndrome, a rare genetic condition linked to autism and social difficulties. Researchers will track developmental milestones, social skills, and behavior using interviews and questionnaires. The goal is to better understand how social impairments change over time, which could help design future treatment trials.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to: If successful, this study could identify key developmental milestones and outcome measures needed to design future clinical trials for potential treatments.
What could go wrong: This is an observational study with only 15 participants, so findings may not apply to everyone with the syndrome. It does not test any treatment directly.

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Conditions

The condition(s) this trial relates to.

7q11.23 microduplication syndrome autism spectrum disorder neurodevelopmental disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

7Q11.23 MICRODUPLICATION SYNDROME (7DUP) AUTISM SPECTRUM DISORDER (ASD NEURODEVELOPMENTAL DISORDERS (NDD)

Contacts and locations

Locations

Developmental Anomalies Reference Center, Genetics Department Woman Mother and Child Hospital, University Hospital of Lyon, Hospices Civils de Lyon
RECRUITING

Bron, 69677, France
Reference Center of Rare Disease with Intellectual Disability- in Lyon, Woman Mother and Child Hospital, University Hospital of Lyon, Hospices Civils de Lyon
RECRUITING

Bron, 69677, France

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