“…Quadricuspid aortic valve (QAV) usually presents as an isolated congenital anomaly, but other associated cardiac anomalies have been reported in about 18-32% of cases including aortic root dilatation [13], tetralogy of Fallot [14], patent ductus arteriosus [15], atrial and ventricular septal defects [16, 17], and anomalous origin of the coronary arteries [12].…”