A comprehensive study of congenital unilateral absence of branch pulmonary artery associated with other congenital heart defects and ipsilateral non-unifocalizable major aorto-pulmonary collateral arteries: A single-center retrospective study
Conclusions: Congenital UAPA is a rare anomaly and associated with a variety of CHDs, TOF being the most common. Single lung corrective surgery in patients with ipsilateral non-unifocalizable MAPCAs has good immediate and long term survival.
Source: Annals of Pediatric Cardiology - Category: Cardiology Authors: H Ravi Ramamurthy Varsha Walavalkar Satheesh Siddaiah Sunita Maheshwari Source Type: research