Klippel-trenaunay-weber syndrome: A case with cerebral and cerebellar hemihypertrophy
✍ Scribed by B. Anlar; K. Yalaz; C. Erzen
- Publisher
- Springer
- Year
- 1988
- Tongue
- English
- Weight
- 105 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0028-3940
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Most cases of KTW syndrome are sporadic. However, in a few, other family members have some clinical manifestations of the syndrome, and an autosomal dominant mode of inheritance has been suggested. In this paper we present a family with an affected child who has large skin hemangiomata, overgrowth o
## 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