Literature DB >> 12796938

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

R Heydanus1, J W Wladimiroff, H Brandenburg, J L Gaillard, P A Stewart, M F Niermeijer.   

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. Copyright 1992 International Society of Ultrasound in Obstetrics and Gynecology

Entities:  

Year:  1992        PMID: 12796938     DOI: 10.1046/j.1469-0705.1992.02050360.x

Source DB:  PubMed          Journal:  Ultrasound Obstet Gynecol        ISSN: 0960-7692            Impact factor:   7.299


  2 in total

1.  Prenatal diagnosis of Klippel-Trenaunay syndrome: Series of four cases and review of the literature.

Authors:  Olga Ivanitskaya; Elena Andreeva; Natalia Odegova
Journal:  Ultrasound       Date:  2019-10-17

2.  Prenatal diagnosis of Klippel-Trenaunay-Weber syndrome with Kasabach-Merritt syndrome in utero.

Authors:  Kei Tanaka; Noriko Miyazaki; Miho Matsushima; Reiko Yagishita; Tomoko Izawa; Shinji Tanigaki; Keiji Sakai; Mitsutoshi Iwashita
Journal:  J Med Ultrason (2001)       Date:  2014-07-03       Impact factor: 1.314

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.