/vitamin K-antagonist embryofetopathy

vitamin K-antagonist embryofetopathy

Rare Disease

MONDO:0016010

Also Known As

di Sala syndromefetal Coumadin syndromefetal warfarin syndromefoetal Coumadin syndromefoetal warfarin syndromevitamin K antagonist embryopathyvitamin K-antagonist embryofetopathyvitamin K-antagonist embryopathywarfarin embryofetopathywarfarin embryopathyDiSala syndromecongenital warfarin syndromecoumarin embryopathycoumarin syndromeembryofetopathy due to oral anticoagulant therapyfetal anticoagulant syndromefoetal anticoagulant syndromevitamin K antagonist embryofetopathyvitamin K antagonists embryofetopathywarfarin syndrome

Definition

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.