Abstract
Anomalous aortic origin of the right coronary artery from the left aortic sinus is a rare congenital anomaly that is generally repaired during adolescence when the condition is associated with symptoms. It is rarely diagnosed in infancy. Similarly, a quadricuspid pulmonary valve is also a rare finding, and there are scant data to evaluate whether this malformation of the pulmonary valve is suitable to be used for a Ross operation. This report describes a case in which both these anomalies coexisted in an infant who underwent a successful Ross-Konno operation.
| Original language | English |
|---|---|
| Pages (from-to) | e41-e43 |
| Journal | The Annals of Thoracic Surgery |
| Volume | 109 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 2020 |
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