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Klippel–Trenaunay syndrome: A multisystem disorder possibly resulting from a pathogenic gene for vascular and tissue overgrowth

Identifieur interne : 007C41 ( Main/Exploration ); précédent : 007C40; suivant : 007C42

Klippel–Trenaunay syndrome: A multisystem disorder possibly resulting from a pathogenic gene for vascular and tissue overgrowth

Auteurs : George G. Kihiczak [États-Unis] ; Jon G. Meine [États-Unis] ; Robert A. Schwartz [États-Unis] ; Camila K. Janniger [États-Unis]

Source :

RBID : ISTEX:65C90A6A0FABC3AEB72CEC251E2CC4ABF3A585B8

Abstract

Klippel–Trenaunay syndrome is characterized by a triad of varicose veins, cutaneous capillary malformation, and hypertrophy of bone and soft tissue. Appropriate evaluation and treatment of children displaying features of the disease may minimize morbidity. The clinical appearance, etiology, genetics, diagnostics, and treatment of Klippel–Trenaunay syndrome are herein explored.

Url:
DOI: 10.1111/j.1365-4632.2006.02940.x


Affiliations:


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