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Klippel-Trenaunay-Weber Syndrome
Definition: A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA), venous malformations (ARTERIOVENOUS FISTULA), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator.

Synonym(s): Klippel-Trenaunay Disease / Disease, Klippel-Trenaunay / Klippel Trenaunay Disease / Klippel Trenaunay Weber Syndrome / Syndrome, Klippel-Trenaunay-Weber
MeSH 2010 © U.S. National Library of Medicine®.
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  Web resources for "Klippel-Trenaunay-Weber Syndrome"
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view the HON description of the site HONcode - Klippel-Trenaunay-Weber Syndromewww.fpnotebook.com  
 
 

Broader term(s): - Angiomatosis - Vascular Diseases - Cardiovascular Diseases

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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy

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Broader term(s): - Cardiovascular Diseases

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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy


  Broader term(s):
      Diseases
          Cardiovascular Diseases
              Vascular Diseases
                  Angiomatosis 

MeSH 2010 © U.S. National Library of Medicine®.

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