Gregory Perens1,*, Takegawa Yoshida2, J. Paul Finn2
Congenital Heart Disease, Vol.17, No.4, pp. 387-392, 2022, DOI:10.32604/chd.2022.021233
- 04 July 2022
Abstract An infant male presented with the rare anatomy consisting of situs solitus, concordant atrioventricular connections to L-looped ventricles, double outlet right ventricle (DORV), and hypoplastic aortic arch. 6 months after
neonatal aortic arch repair, the morphologic right ventricle function deteriorated, and surgical evaluation was
undertaken to determine if either biventricular repair with a systemic morphologic left ventricle or right ventricular exclusion was possible. After initial echocardiography, magnetic resonance imaging (MRI) was used to create detailed axial and 4-dimensional (4D) images and 3-dimensional (3D) printed models. The detailed anatomy
of this rare, complex case and its More >
Graphic Abstract
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