William N. Evans1,2, Ruben J. Acherman1,2, Dean Berthoty3, Gary A. Mayman1,2, Michael L. Ciccolo1,4, Sergio A. Carrillo1,4, Humberto Restrepo1,2
Congenital Heart Disease, Vol.13, No.4, pp. 624-627, 2018, DOI:10.1111/chd.12623
Abstract Patients: We reviewed all patients evaluated at our center with situs solitus, levocardia, and a right
aortic arch that were born between January 2000 and January 2018. Results: From our databases,
we identified 204 patients. We excluded patients with a double aortic arch from analysis. Of the
204 patients, 103 (50%) were male. Of the 204 patients, 95 (47%) had an isolated right aortic arch.
Of the 95 with an isolated right aortic arch, 4 (4%) had chromosome 22q11.2 deletion syndrome,
and 89 (94%) had a vascular ring. Of the 204 patients, 109 (53%) had a surgical intracardiac malformation. Of… More >
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