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Ann Thorac Surg 1987;44:154-158
© 1987 The Society of Thoracic Surgeons
Departments of Surgery and Pediatrics, Arkansas Children's Hospital and University of Arkansas for Medical Sciences, Little Rock, AR
Accepted for publication December 30, 1986.
* Address reprint requests to Dr. Westerman, Arkansas Children's Hospital, 800 Marshall St, Little Rock, AR 72202
Double-outlet right ventricle and severe systemic outflow tract hypoplasia comprises a subset of patients in whom total correction or palliation requires complex surgical procedures in the neonatal period. Our experience with 3 patients illustrates the difficulties associated with treatment and suggests possible surgical options for this otherwise lethal variant of the Taussig-Bing syndrome.
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