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
Deviated nasal septum in case of Klippel-Trenaunay-Weber Syndrome
✍ Scribed by Rajesh; S. S. Bist; R. K. Saxena
- Publisher
- Springer
- Year
- 2006
- Tongue
- English
- Weight
- 809 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0019-5421
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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
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