Abstract：
:A 2 year old boy with ventricular inversion and normal ventriculoarterial connection is described. Associated cardiac lesions included single atrium, absence of the coronary sinus, bilateral superior venae cavae, absence of the hepatic segment of the inferior vena cava with azygos and hemiazygos continuation, right aortic arch, levocardia and left atrial isomerism. At 5 days of age, the patient underwent a Waterston (aortopulmonary) anastomosis because of suspected pulmonary atresia. The correct diagnosis was established at 2 years of age and the patient had a successful Mustard operation (interatrial baffle procedure) and closure of the Waterston anastomosis. Accurate preoperative diagnosis is difficult in this rare cardiac anomaly and the reported mortality rate is high.
journal_name
J Am Coll Cardioljournal_title
Journal of the American College of Cardiologyauthors
Park SC,Siewers RD,Neches WH,Mathews RA,Fricker FJ,Beerman LB,Fischer DR,Zuberbuhler JRdoi
10.1016/s0735-1097(84)80331-9subject
Has Abstractpub_date
1984-07-01 00:00:00pages
136-40issue
1eissn
0735-1097issn
1558-3597pii
S0735-1097(84)80331-9journal_volume
4pub_type
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