Klippel-Trénaunay-Weber syndrome associated with fetal growth restriction
- PMID: 8981152
- DOI: 10.1093/oxfordjournals.humrep.a019156
Klippel-Trénaunay-Weber syndrome associated with fetal growth restriction
Abstract
Klippel-Trénaunay-Weber syndrome is a rare congenital deep-vein malformation. Pregnancy in patients with this syndrome is rare and only a few cases have been reported. Known obstetrical risks in pregnant patients with this syndrome include bleeding from angiomata in the genitalia, and coagulation disturbances. We present a 31 year old woman with this syndrome who, on two occasions, delivered small-for-gestational-age neonates. This may have been due to placental insufficiency caused by angiomatosis related to the syndrome.
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