Fetal warfarin syndrome
| Fetal warfarin syndrome | |
|---|---|
 | |
| Classification and external resources | |
| Specialty | Teratology |
| ICD-10 | Q86.0 |
| ICD-9-CM | 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 "DiSaia 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 intellectual disability, seizures, reduced muscle tone, widely spaced nipples, deafness and feeding difficulty.
External links
References
- ↑ 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.
- ↑ Hou JW (September 2004). "Fetal warfarin syndrome" (PDF). Chang Gung Med J 27 (9): 691–5. PMID 15605910.
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