Key result
Two siblings with atrial septal defects and dysplasia of the mitral and tricuspid valves exhibited abnormal ventricular activation, likely due to an accessory nodoventricular pathway.
Case Report (n=2)
Dysplasia of the atrioventricular valves combined with hypoplasia of the central fibrous body and accessory pathways may represent a specific malformative complex caused by incomplete differentiation.
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May warrant accessory pathway evaluation in familial ASD with valve dysplasia; leaves open whether this forms a distinct heritable malformative complex.
Clinical, vectorcardiographic, and echocardiographic data from two siblings with atrial septal defects and dysplasia of the mitral and tricuspid valves are reported. Vectorcardiograms showed that both siblings had abnormal ventricular activation with initial electrical forces directed posteriorly. One sibling died after surgery, and necropsy showed incomplete differentiation of the leaflets and tensor apparatus producing anomalies resembling "mitral arcade." Serial histological examination of the conducting tissue showed that the atrioventricular node was located on the left side of the atrial septum, that the central fibrous body and the membranous septum were hypoplastic, and that an accessory nodoventricular pathway originating in the compact node joined the left side of the ventricular septum. This accessory pathway was probably the cause of the unusual ventricular activation. Dysplasia of the mitral and tricuspid valves together with hypoplasia of the central fibrous body and the presence of accessory pathways are probably part of a malformative complex caused by incomplete differentiation of both the cardiac atrioventricular valves and the junctional area.
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Daliento et al. (1984) conducted a case report in Atrial septal defects and dysplasia of the mitral and tricuspid valves (n=2). Dysplasia of the atrioventricular valves and conduction system anomalies was evaluated. Two siblings with atrial septal defects and dysplasia of the mitral and tricuspid valves exhibited abnormal ventricular activation, likely due to an accessory nodoventricular pathway.
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