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Klippel–Trenaunay syndrome associated with polydactyly

Identifieur interne : 007C42 ( Main/Exploration ); précédent : 007C41; suivant : 007C43

Klippel–Trenaunay syndrome associated with polydactyly

Auteurs : Hasan Sunar [Turquie] ; Umit Halici [Turquie] ; Enver Duran [Turquie]

Source :

RBID : ISTEX:6F74C8124BE0451B4C040494396E39B2B74CE4F6

Abstract

Klippel–Trenaunay syndrome (KTS) manifests cutaneous vascular nevus, superficial venous varicosities, and hypertrophy of the affected limb. KTS may be associated with other developmental anomalies such as polydactyly, syndactyly, and macrocephaly. We present a case with KTS associated with polydactyly. Clin. Anat. 19:78–81, 2006. © 2005 Wiley‐Liss, Inc.

Url:
DOI: 10.1002/ca.20176


Affiliations:


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