Clin2
NCT05731141Possibly a fitRecruiting

Study of lymphatic birthmarks and related genetic conditions

Lymphatic DiseasesLymphatic Abnormalities

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.

Phase
N/A
Enrollment
1,200 people
Ages
1 day to 100 years
Study type
Observational

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

View the official record on ClinicalTrials.gov

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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