Fetal warfarin syndrome

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Fetal warfarin syndrome
Classification and external resources
ICD-10 Q86.0
ICD-9 760.7
DiseasesDB 33178

Fetal warfarin syndrome (Dysmorphism due to warfarin, Warfarin embryopathy ) is a condition associated with administration of Warfarin during pregnancy.[1]

Associated conditions include hypoplasia of nasal bridge, laryngomalacia, pectus carinatum, congenital heart defects, ventriculomegaly, agenesis of the corpus callosum, stippled epiphyses, telebrachydactyly, and growth retardation.[2]

It is also known as "DiSala syndrome". The symptoms are Nasal hypoplasia, Depressed nasal bridge, Deep groove between nostril and nasal tip, Stippling of uncalcified epiphyses during first year, Mild hypoplasia of nails, Shortened fingers, Low birth weight, Significant mental retardation, Seizures, Reduced muscle tone, Widely spaced nipples, Deafness, Feeding difficulty, Failure to thrive

External links[edit]


  1. ^ Raghav S, Reutens D (February 2007). "Neurological sequelae of intrauterine warfarin exposure". J Clin Neurosci 14 (2): 99–103. doi:10.1016/j.jocn.2006.03.031. PMID 17107801. 
  2. ^ Hou JW (September 2004). "Fetal warfarin syndrome". Chang Gung Med J 27 (9): 691–5. PMID 15605910.