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Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery: A Case Report

This case report presents a four month old infant with anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) syndrome including clinical presentation of severe cardiomyopathy and left-sided heart failure. Child was operated for reimplantation of ALCAPA to aortic root with satisfactory outcome.


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