Study of lymphatic birthmarks and related genetic conditions
Part of Blood & lymphatic, Bones, joints & muscles, Digestive system, Genetic & congenital clinical trials.
This study follows people who have lymphatic anomalies (lymphatic birthmarks) and sometimes related vascular or genetic conditions. It aims to better understand how these problems develop and what genetic causes may be involved.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have a current or past lymphatic anomaly, or symptoms that could be a lymphatic problem
- Or you have a vascular anomaly that may also involve the lymphatic system
- Or you have a genetic result (pathogenic, likely pathogenic, or VUS) linked to a syndrome with lymphatic problems
- Or you have been diagnosed with a syndrome known to involve lymphatic issues
- If you’re a parent or sibling of an affected person, you must be a first-degree family member
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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