Persistent left fifth aortic arch in a child without congenital heart disease: Echocardiographic and magnetic imaging correlation

R. Steelman, L. A. Pyles, A. Balian, E. Millman, P. McLaughlin, S. Einzig

Research output: Contribution to journalArticle

Abstract

Persistence of the left fifth aortic arch is rare. The first reported case was by Van Praagh et al and since then, there have been about 16 additional case reports. All of these cases had associated cardiac lesions such as tricuspid atresia, ventricular septal defect, transposition of the great arteries, coarctation of the aorta, pulmonary atresia, or patent ductus arteriosus. The purpose of this report is to document the presence of a left fifth arch in a patient without structural cardiac disease.

Original languageEnglish (US)
Pages (from-to)46-48
Number of pages3
JournalCardiovascular Reviews and Reports
Volume20
Issue number1
StatePublished - Jan 1 1999

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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