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Article in English | IMSEAR | ID: sea-89204

ABSTRACT

Klippel-Trénaunay syndrome (KTS) is an uncommon entity. This congenital malformation is characterized by the triad of soft tissue or bony hypertrophy, cutaneous vascular malformations, and atypical venous abnormalities. We report here a case of KTS and discuss the clinical features, investigations, and management of this enigmatic condition.


Subject(s)
Adolescent , Anti-Bacterial Agents/therapeutic use , Blood Transfusion , Diagnosis, Differential , Enoxaparin/therapeutic use , Humans , Klippel-Trenaunay-Weber Syndrome/diagnosis
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