Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome study
Part of Bones, joints & muscles, Heart & circulation clinical trials.
This study looks at children with CACP syndrome, a rare genetic condition, to learn more about how the condition affects the body over time.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You must have a clinical diagnosis of CACP syndrome that has been confirmed by genetic testing.
- You must have been diagnosed with CACP during childhood (before age 18).
- You must have been diagnosed between January 2005 and January 1, 2026.
- Your parent or legal guardian must give permission for you to take part in 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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