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Truncus arteriosus and double aortic arch associated with DiGeorge syndrome
G Pacileo1, G Palma, M G Russo
1Department of Pediatric Cardiology, Medical and Surgical Institute of Cardiology, 1st Medical School Hospital "Monaldi," Naples, Italy.
Texas Heart Institute Journal
|January 1, 1991
Abstract:
We report the 1st known case in which truncus arteriosus and double aortic arch have been associated with DiGeorge syndrome. The association of these 2 cardiovascular anomalies lends support, by itself, to speculation that truncus arteriosus and double aortic arch have a common embryonic pathogenesis; and the presence of these anomalies in a patient with DiGeorge syndrome strengthens the contention that the common causative factor is pathologic development of the neural crest cells.