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Double aortic arch with aortic atresia and left-sided type B interruption

  • Carissa M. Baker-Smith
  • , Angelo S. Milazzo
  • , Donald P. Frush
  • , James Jaggers
  • , Margaret L. Kirby
  • , Ronald J. Kanter
  • , Piers C. Barker
  • Duke University

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Aortic valve atresia with interruption of the aortic arch is an extremely rare anomaly; only eleven cases of this anomaly have been reported to date. In the absence of additional sources of blood flow to the ascending aorta, aortic valve atresia with interruption of the aortic arch is fatal. We present, to the best of our knowledge, the first case of a live birth with aortic valve atresia and interrupted left aortic arch (type B) without evidence of an aorticopulmonary communication or ductal supply to the native ascending aorta. Instead, blood flow to the native aortic root was derived from a persistent right embryonic dorsal aorta.

Original languageEnglish
Pages (from-to)316-320
Number of pages5
JournalCongenital Heart Disease
Volume5
Issue number3
DOIs
StatePublished - 2010
Externally publishedYes

Keywords

  • Embryonic Arch
  • Interrupted Aortic Arch
  • Ventricular Septal Defect

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