“…Although narrowing of the aortic arch is not infrequently seen in the setting of congenital heart surgery, aortic coarctations that persist into adult life are unusual, and those that originate between the arch vessels are very rare, constituting approximately 1% of all coarctation cases. [4][5][6][7][8] Although aortic coarctation often occurs as an isolated malformation, it is also associated with a bicuspid valve in up to 85% of patients and also with other associated anomalies, including left heart obstructive lesions, congenital abnormalities of Brief Communications the mitral valve, ventricular septal defects, and patent ductus arteriosus. The pathogenesis of the stenosis is not well understood but seems to involve at least 2 mechanisms.…”