Annals of Pediatric Cardiology
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Case of anomalous origin of right coronary artery from pulmonary artery associated with interrupted aortic arch type A, diagnosed by multidetector computed tomography angiography

1 Department of Radiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
2 Department of Neurology, Great Plains Health, North Platte, Nebraska, USA
3 Department of Medicine, Great Plains Health, North Platte, Nebraska, USA
4 Department of Radiology, YaleNew Haven Health Bridgeport Hospital, Bridgeport, Connecticut, USA

Correspondence Address:
Anil Kumar,
Department of Neurology, Great Plains Health North Platte, Nebraska
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/apc.APC_69_18

Anomalous origin of the right coronary artery from pulmonary artery (ARCAPA) is a rare congenital anomaly of the coronary circulation, which can be easily missed by echocardiography. Interrupted aortic arch (IAA) is another rare congenital cardiac abnormality that typically presents in the first few weeks of life. We present a case of ARCAPA associated with IAA diagnosed with the help of multidetector computed tomography angiography, in a 7-year-old boy.

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