Abstract
The ingenious contribution of Fontan and Baudet [35] has forever altered the natural history of the patient with functionally one ventricle. The application of an atriopulmonary connection and atrial partitioning to a patient in 1968 with tricuspid atresia opened the doors to potential longterm palliation for patients with a wide range of complex cardiac malformations [25, 60, 69]. This operation has effectively removed for many children the “Cinderella” stigma [17]. We will explore the clinical manifestations of the neonate with single ventricle, those methodologies that are diagnostic of this condition, and those surgical procedures that palliate and preserve the potential for Fontan’s operation. See also Chapter 19.
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Freedom, R.M., Smallhorn, J.F. (1992). Hearts with a Univentricular Atrioventricular Connection. In: Neonatal Heart Disease. Springer, London. https://doi.org/10.1007/978-1-4471-1814-5_30
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