Williams syndrome and related 7q11.23 changes study
Part of Brain & nervous system, Genetic & congenital, Heart & circulation, Mental health clinical trials.
This study follows people with Williams syndrome, 7q11.23 duplication, or related genetic changes over time to understand how these conditions affect health and development. It also includes close family members to learn about the genetics.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have Williams syndrome (confirmed by a doctor or genetic test), or
- You are a biological parent or sibling of someone with Williams syndrome, or
- You have a genetic test showing 7q11.23 duplication syndrome, or
- You have a different genetic change in the 7q11.23 region
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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