Studying genes in neurodevelopmental disorders with birth defects
Part of Mental health clinical trials.
This study is for children or adults with neurodevelopmental conditions and unusual physical features, where standard genetic tests haven't found a cause. Researchers will use RNA and DNA sequencing to look for hidden genetic explanations, which could guide better care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Must have a neurodevelopmental disorder with intellectual disability, developmental delays, autism, or ADHD.
- Must have physical differences or birth defects (dysmorphism or developmental anomalies).
- Previous genetic tests (like CMA or exome) must have been negative (no cause found).
- Must be willing to provide a skin biopsy or already have a sample available.
- Must be able to give consent (parent/guardian for minors or adults unable to consent).
- Must be affiliated with French national health coverage or equivalent.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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