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Repair of TGA-type DORV (Taussig-Bing anomaly) entails creation of an autologous pericardial ba e between the LV and the pulmonary valve (the semilunar valve closer to the VSD) and an arterial switch operation (see Chapter ˛). Aortic arch hypoplasia or aortic coarctation are not unusual in this setting, requiring arch reconstruction in
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