## Abstract This report describes the prenatal sonographic diagnosis of a case of Klippel‐Trénaunay‐Weber syndrome. The sonographic appearance of this disorder was characterized by the presence of multiple distorted cystic areas involving the right leg and abdomen and cardiomegaly with early fetal
Sonographic identification of lower limb venous hypoplasia in the prenatal diagnosis of Klippel–Trénaunay syndrome
✍ Scribed by P. R. Coombs; P. A. James; A. G. Edwards
- Book ID
- 112229450
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 162 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0960-7692
- DOI
- 10.1002/uog.7461
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Ultrasound examination led to prenatal diagnosis of Klippel-Trénaunay-Weber syndrome complicated by early fetal congestive heart failure. The postnatal course was complicated by the Kasabach-Merritt syndrome of thrombocytopenia due to platelet consumption within the haemangioma. There was need for n
Klippel-Trenaunay-Weber syndrome is a complex developmental disorder characterized by a triad of cutaneous haemangioma, varicosities of the body, and unilateral limb hypertrophy. We describe the prenatal diagnosis of Klippel-Trenaunay-Weber syndrome at 15 weeks' gestation using the surface rendering