“…In non-heterotaxy cases, TAPVC can be detected as an isolated anomaly or with other complex heart/great vessel lesions such as atrioventricular septal defect, transposition of the great arteries, pulmonary stenosis, double outlet right ventricle, and coarctation of the aorta. When TAPVC is diagnosed through prenatal echocardiography, a trend of more fetuses accompanied with heterotaxy syndrome or complex CHD and less fetuses with isolated TAPVC has been noted [ 24 ]. TAPVC genetic etiology is remaining vogue and previous study reported some possible disease-driven genes (e.g., ACVRL1, SGCD , 4p13-q12, ANKRD1 , etc.)…”