Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a serious congenital heart defect, typically existing on its own and rarely linked to other heart issues.
The report discusses a successful surgical repair in an infant with a rare combination of ALCAPA, a ventricular septal defect (VSD), and a double aortic arch (DAA).
This case is notable as it is only the second documented instance of ALCAPA occurring alongside VSD and DAA in medical literature.