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Hofer, T., Frank, J. and Itin, P.H. (2005) Klippel-Trenaunay Syndrome in a Monozygotic Male Twin: Supportive Evidence for the Concept of Paradominant Inheritance. European Journal of Dermatology, 15, 341-343.

has been cited by the following article:

• TITLE: Pregnancy and Klippel-Trenaunay Syndrome—A Case Report

  AUTHORS: María Jesús Cancelo Hidalgo, Gisselle Adriana González Segura, Laura Yago Lisbona, Estherde la Viuda García

  KEYWORDS: Klippel-Trenaunay Syndrome, Pregnancy

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.3 No.7, July 23, 2014

  ABSTRACT: Klippel-Trenaunay Syndrome (KTS) is a rare triad of congenital vascular malformations involving extensive Port wine stains, soft tissue or bone hypertrophy and underlying venous and/or lymphatic malformation affecting limb, pelvicor abdominal organs. Pregnancy is known to exacerbate KTS complications and can put women at increased obstetrical risk due to deep venous thrombosis and other thromboembolic events. We report a case of a pregnant woman with KTS with the personal antecedent of two episodes of pulmonary thromboembolism.