Literature DB >> 20576054

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

Carissa M Baker-Smith1, Angelo S Milazzo, Donald P Frush, James Jaggers, Margaret L Kirby, Ronald J Kanter, Piers C Barker.   

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.

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Year:  2010        PMID: 20576054     DOI: 10.1111/j.1747-0803.2009.00341.x

Source DB:  PubMed          Journal:  Congenit Heart Dis        ISSN: 1747-079X            Impact factor:   2.007


  1 in total

1.  Collateral dependent cerebral and coronary circulation in a newborn.

Authors:  Dilek Suzan; Selim Aydin; Ibrahim Halil Demir; Ersin Erek
Journal:  Indian J Thorac Cardiovasc Surg       Date:  2020-01-27
  1 in total

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