Introduction
Congenitally corrected transposition of the great arteries (cc-TGA) is a rare type of congenital heart disease with an incidence of less than 1% of infants with congenital heart disease1. Other terms have been used to describe this congenital anomaly such as L-TGA, double discordance and ventricular inversion. The first heart-lung transplantation (HLTx) was performed at Stanford University in 1981.2 Pulmonary vascular disease and cystic fibrosis were the main indications for HLTx initially. However, in the recent years, the indication has been expanded to include congenital heart disease and idiopathic pulmonary artery hypertension.3We report a rare case of cc-TGA with dextrocardia presenting with biventricular failure who underwent HLTx.