*Corresponding author:
Gian Manuel Jiménez-Rodríguez, Instituto Nacional de Cardiología, Ignacio Chávez, Ciudad de, MéxicoReceived: April 13, 2018; Published: April 25, 2018
DOI: 10.26717/BJSTR.2018.04.001000
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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
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