blepharocheilodontic syndrome

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
CDH1-associated Blepharocheilodontic Syndrome Registry	Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mouth Abnormalities, Skin Abnormalities, Skin and Connective Tissue Diseases, Stomatognathic Diseases, Stomatognathic System Abnormalities, blepharocheilodontic syndrome, cleft lip, ectodermal dysplasia syndrome, hereditary disease, hereditary skin disorder, lip disorder, mouth disorder, skin disorder	Recruiting	Not stated	2025-08-21		NCT07133464

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