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Isolated type a interrupted aortic arch: in an asymptomatic 19-year-old man
Baris Bugan1, Atila Iyisoy, Murat Celik
1Department of Cardiology, Gulhane Medical Academy, 06018 Ankara, Turkey.
Abstract:
Interrupted aortic arch, characterized by luminal and anatomic discontinuity between the ascending and descending aorta, is a very rare congenital malformation. The condition is typically diagnosed in neonates and is highly fatal if left untreated. Herein, we report the unusual diagnosis of an isolated type A interrupted aortic arch in a hypertensive, asymptomatic 19-year-old man.
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