Double-orifice mitral valve (DOMV) is an uncommon congenital anomaly account for 1% of congenital heart disease. However, accurate diagnosis and evaluation of valve stenosis or regurgitation and other concomitant congenital anomalies due to DOMV are required to obtain suitable treatment. Two- and three-dimensional echocardiography can contribute valuable functional and anatomic information that can support to reach this goal. Here, we present a case of complete bridge-type DOMV that causes mitral stenosis after surgical repair of the partial atrioventricular septal defect in childhood.

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http://dx.doi.org/10.1111/echo.14688DOI Listing

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Article Synopsis
  • Shone's syndrome (SS) is a rare congenital heart defect with a range of developmental issues.
  • It mainly features left ventricular inflow and outflow tract lesions, including parachute mitral valve and supravalvular mitral ring.
  • Cases involving a double-orifice mitral valve in Shone's syndrome are not commonly reported.
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