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Double aortic arch: an unusual congenital variation
K S Satyapal1, L Lazarus, D Shama
1Department of Clinical Anatomy, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, Westville Campus, University of KwaZulu-Natal, Private Bag X54001, Durban, 4001, South Africa. satyapalk@ukzn.ac.za
Double aortic arch, a rare congenital vascular anomaly, can compress the trachea and esophagus. Surgical correction in two pediatric patients successfully resolved symptoms like stridor and respiratory infections, leading to full recovery.
Area of Science:
- Cardiology
- Pediatric Surgery
- Medical Imaging
Background:
- Double aortic arch is a rare congenital anomaly of the aortic arch.
- This vascular variation can lead to significant tracheal and esophageal compression in infants and children.
- Symptoms include stridor, recurrent respiratory infections, and apneic episodes.
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