CDH1 gene and BCDS syndrome registry
Part of Genetic & congenital, Mouth & dental, Skin clinical trials.
This registry studies people with changes in the CDH1 gene who may have blepharocheilodontic syndrome (BCDS). It collects information to better understand the condition and improve care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have a confirmed change (mutation) in the CDH1 gene.
- You have at least one sign of BCDS, like cleft lip or palate, eyelid issues, dental problems, webbed toes, or a blocked anus.
- You are able to speak and read English.
- You are willing to share your medical information for research.
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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