Concept:
Tricuspid atresia is a cyanotic congenital heart lesion characterized by complete agenesis of the tricuspid valve, leading to absent direct communication between the right atrium and right ventricle.
It produces a classic electrocardiographic signature that uniquely separates it from nearly all other cyanotic heart defects in neonates.
Explanation:
• In normal neonates, right ventricular dominance produces a physiological right axis deviation (RAD) and right ventricular hypertrophy (RVH) on ECG.
• In tricuspid atresia, systemic venous blood in the right atrium must shunt right-to-left through an obligatory ASD/PFO into the left atrium, where it mixes with pulmonary venous blood and enters the dominant left ventricle.
• Because the right ventricle is hypoplastic and the left ventricle handles total systemic and pulmonary cardiac output, the neonatal ECG characteristically demonstrates Left Axis Deviation (LAD, typically $-30^\circ\text{ to }-90^\circ$) and Left Ventricular Hypertrophy (LVH).
• Chest radiography shows decreased pulmonary vascular markings (oligemic lung fields) because of severe subpulmonary stenosis or pulmonary atresia.
• By comparison, Tetralogy of Fallot, TGA, and Truncus arteriosus exhibit right axis deviation and right ventricular dominance on neonatal ECG.
Final Answer:
A cyanotic neonate with decreased pulmonary blood flow and an ECG demonstrating left axis deviation with LVH has the hallmark findings of Tricuspid Atresia.