Study families with genetic RAS syndromes, including adults and children
Part of Bones, joints & muscles, Genetic & congenital, Heart & circulation, Skin clinical trials.
This study looks at people with certain inherited genetic conditions called RASopathies and their family members. It helps researchers understand these conditions and how genetic changes run in families, which may improve future care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You (or your child) have a known RASopathy diagnosis or a related gene change
- Your genetic result must be in a RAS-pathway gene (or your doctor suspects a RASopathy and testing is done as part of the study)
- You cannot have only an NF1 (neurofibromatosis type 1) diagnosis unless you also have another RASopathy
- You must be willing to return for follow-up visits and complete required study tests
- You (or a legal representative) must sign informed consent for the study
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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