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

作者信息

Heydanus R, Wladimiroff J W, Brandenburg H, Gaillard J L, Stewart P A, Niermeijer M F

机构信息

Department of Obstetrics and Gynecology, Academic Hospital Rotterdam-Dijkzigt, The Netherlands.

出版信息

Ultrasound Obstet Gynecol. 1992 Sep 1;2(5):360-3. doi: 10.1046/j.1469-0705.1992.02050360.x.

Abstract

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.

摘要

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