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The Journal of Thoracic and Cardiovascular Surgery, Vol 81, 239-244, Copyright © 1981 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
WI Norwood and GJ Stellin
Aortic atresia is a form of congenital cardiac disease always complicated
by associated severe hypoplasia of the ascending aorta and various degrees
of mitral valve and left ventricular hypoplasia. Rarely, there is an
associated ventricular septal defect (VSD) and, consequently, a
well-developed left ventricle. This complex malformation is universally
lethal and survived after a reparative operation has not been previously
reported. The following is an account of an infant with aortic atresia,
VSD, and Type C aortic arch interruption who presented with a unique
ductus-dependent physiology and is clinically well 11 months following a
reparative operation.
ARTICLES
Aortic atresia with interrupted aortic arch: reparative operation
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