Klippel-Trenaunay-Weber Syndrome Index

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Klippel-Trènaunay-Weber (KTW) syndrome is a condition characterized by port-wine stains or birthmark malformations in the skin, soft tissue and bony growths (generally involving a limb), and vascular anomalies (varicose veins). The cause of Klippel-Trènaunay-Weber syndrome is not known, however, recently, there have been some cases that run in families. There is no significant treatment for Klippel-Trènaunay-Weber syndrome.

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Terms related to Klippel-Trenaunay-Weber Syndrome:

  • Congenital Dysplastic Angiectasia
  • Elephantiasis Congenita Angiomatosa
  • Hemangiectatic Hypertrophy
  • KTS
  • KTW
  • Osteohypertrophic Nevus Flammeus
  • Angio-Osteohypertrophy Syndrome

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