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Vitamin K-antagonist embryofetopathy
rareA 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.
- Identifiers
- MONDO:0016010 Orphanet:1914
- Also known as
- congenital warfarin syndrome · coumarin embryopathy · coumarin syndrome · di Sala syndrome · DiSala syndrome
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