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ISSN: 2574 -1241
ISSN: 2574 -1241
Received: April 13, 2018; Published: April 25, 2018
DOI: 10.26717/BJSTR.2018.04.001000
Klippel-Trenaunay-Weber syndrome is a rare congenital disorder characterized by the triad of capillary malformations, bony or soft tissue hypertrophy usually of lower limbs, and venous varicosities or malformations [1], both genders are equally affected. The prevalence is estimated 1 in 20 000 to 1 in 100 000 live births [2].
Abbrevation: KTWS: Klippel Trenaunay Weber Syndrome; LA: Left Atrium; LVHY: Left Ventricular Hypokinesia; EF: Ejection Fraction
Introduction| Case Report| Discussion| Conclusion| References|
International Association of Landscape Archaeology, Czech Glass Society, Czech Republic
Department of Chemistry, Semenov Institute of Chemical Physics, USSR Academy of Sciences, Moscow, Russia
Pharmaco-kinetics, dynamics and Drug Metabolism, Touro College of Pharmacy, USA
Professor of Nuclear Medicine, Faculty of Medicine and Surgery, University of Milan, Milan, Italy
Associate Professor at Department of Breast and Thyorid Surgey, Chongqing General Hospital, China
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