Abstract
Berry syndrome, which consists of distal aortopulmonary septal defect (APSD), aortic origin of the right pulmonary artery, interrupted aortic arch, intact ventricular septum, and patent ductus arteriosus, is an extremely uncommon congenital cardiac malformation, with only 25 cases having been reported since the first report in 1982. Here we report the first case of Berry syndrome complicated by anomalous origin of the left coronary artery from the main pulmonary artery. The possibility of coronary anomaly should be seriously considered in all cases of Berry syndrome.
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More From: The Journal of Thoracic and Cardiovascular Surgery
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