Aortic atresia with interrupted aortic arch is a rare and critical congenital cardiac anomaly. We report a unique case of Type B interruption with aortic atresia, in which cerebral and coronary perfusion were solely dependent on the left vertebral artery without alternative circulatory pathways within the thoracic cavity. The patient underwent successful single-stage biventricular repair and continues to demonstrate favorable neurodevelopmental progress.
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Kalithkar et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69b5ff6e83145bc643d1bfcd — DOI: https://doi.org/10.1177/21501351261423197
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Anusha Bai Kalithkar
Juanita Montoya Arango
Phillip Zegelbone
World Journal for Pediatric and Congenital Heart Surgery
University of Miami Hospital
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