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Klippel-Trenaunay syndrome: A rare cause of severe headache

✍ Scribed by Abraham J. Sorom; David Driscoll; Anthony Stanson


Publisher
Springer
Year
2011
Tongue
English
Weight
626 KB
Volume
11
Category
Article
ISSN
1061-1711

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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

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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