Author:
Mahdavi Mohammad,Vahidshahi Koorosh,Tehrani Ramin Baghai,Ali-Akbar Hamidreza Poor,Godarzi Mohammad Rad
Abstract
AbstractAnomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a very rare congenital heart anomaly. Most of the cases are asymptomatic during infancy and childhood. We report ARCAPA associated with aberrant right subclavian artery in a 2-month male infant presenting with heart failure. We used computed tomography angiography for confirming the diagnosis and also for post-operative follow-up.
Publisher
Cambridge University Press (CUP)
Subject
Cardiology and Cardiovascular Medicine,General Medicine,Pediatrics, Perinatology and Child Health
Cited by
3 articles.
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