Klippel–Trenaunay syndrome: A multisystem disorder possibly resulting from a pathogenic gene for vascular and tissue overgrowth
Identifieur interne : 002F62 ( Istex/Curation ); précédent : 002F61; suivant : 002F63Klippel–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 :
- International Journal of Dermatology [ 0011-9059 ] ; 2006-08.
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.
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DOI: 10.1111/j.1365-4632.2006.02940.x
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<front><div type="abstract" xml:lang="en">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.</div>
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