Prenatal diagnosis of Klippel-Trenaunay-Weber syndrome: a case report. 1992

R Heydanus, and J W Wladimiroff, and H Brandenburg, and J L Gaillard, and P A Stewart, and M F Niermeijer
Department of Obstetrics and Gynecology, Academic Hospital Rotterdam-Dijkzigt, The Netherlands.

At 20 weeks of gestation, a typical combination of a massive enlargement of the right fetal leg and multiple cystic lesions was detected at ultrasound examination. Color-coded Doppler examination revealed no arteriovenous fistulae. These findings allowed an in utero diagnosis of the Klippel-Trenaunay-Weber syndrome, which was confirmed after subsequent termination of the pregnancy. The severe malformation involved the upper and lower right leg. No arteriovenous fistulae were found.

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