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

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...

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Main Authors: A.A. Konyushevskaya (Author), S.Ya. Yaroshenko (Author)
Format: Book
Published: Zaslavsky O.Yu., 2014-03-01T00:00:00Z.
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500 |a 2224-0551 
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500 |a 10.22141/2224-0551.2.53.2014.75957 
520 |a 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. 
546 |a EN 
546 |a UK 
690 |a Klippel-Trenaunay-Weber-Rubashov syndrome 
690 |a children 
690 |a Pediatrics 
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786 0 |n Zdorovʹe Rebenka, Vol 9, Iss 2.53, Pp 117-122 (2014) 
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