Clinical Case of Rare Hereditary Pathology — Klippel-Trenaunay-Weber-Rubashov Syndrome in Pediatrician’s Practice

Journal Title: Здоров`я дитини - Year 2014, Vol 2, Issue 53

Abstract

The article deals with the study of clinical and morphological features of Klippel-Trenaunay-Weber-Rubashov syndrome (cutaneous angiomas, superficial veins dilatation, hypertrophy of affected extremity, arteriovenous anastomoses). The data about the nature, pathogenetic mechanisms, the prevalence of the syndrome are given, a typical clinical case is considered.

Authors and Affiliations

A. A. Konyushevskaya, S. Ya. Yaroshenko

Keywords

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  • EP ID EP311130
  • DOI -
  • Views 44
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How To Cite

A. A. Konyushevskaya, S. Ya. Yaroshenko (2014). Clinical Case of Rare Hereditary Pathology — Klippel-Trenaunay-Weber-Rubashov Syndrome in Pediatrician’s Practice. Здоров`я дитини, 2(53), 117-122. https://europub.co.uk/articles/-A-311130