Fetal warfarin syndrome

Fetal warfarin syndrome
Classification and external resources

Warfarin
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".

References

  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. http://linkinghub.elsevier.com/retrieve/pii/S0967-5868(06)00334-1. 
  2. ^ Hou JW (September 2004). "Fetal warfarin syndrome". Chang Gung Med J 27 (9): 691–5. PMID 15605910. http://memo.cgu.edu.tw/cgmj/2709/270908.pdf. 
Congenital malformation due to exogenous toxicity (Q86, 760.7)
Alcohol
Other

Happens when McDonagh and Ciaran Smith have Ginger babies also described as ginger syndrome