Vitamin K-antagonist embryofetopathy

A teratogenic disorder observed in a newborn or child of a mother who was exposed to warfarin during pregnancy. Manifestations include nasal bridge depression, nasal bones hypoplasia, microcephaly, congenital heart disorders, and brachydactyly.

Also known as: di Sala syndrome, fetal Coumadin syndrome, fetal warfarin syndrome, foetal Coumadin syndrome, foetal warfarin syndrome, vitamin K antagonist embryopathy, vitamin K-antagonist embryofetopathy, vitamin K-antagonist embryopathy

0 clinical trials for this condition and its sub-types, 0 tagged with Vitamin K-antagonist embryofetopathy itself.