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...
A heart is described pathologically in which the aorta emerged from the right ven-tricle and was not...
The case of an infant with double outlet right ventricle with anatomically corrected malposition of ...
Biventricular repair in right atrial isomerism is rarely feasible due to associated anomalies of ven...
A 2 year old boy with ventricular inversion and normal ventriculoarterial connection is described. A...
Aortic atresia associated with ventriculoarterial discordance (transposition) was found at necropsy ...
Aortic atresia is rare in the setting of a normally developed left ventricle with a ventricular sept...
AbstractGross morphologic study of 14 hearts with congenitally corrected transposition or discordant...
A child presented at birth with severe cyanosis. Echocardiography showed hypoplasia of the right hea...
An isolated right superior vena cava (RSVC) draining into the left atrium represents a very rare con...
Atrial isomerism is very rare in adolescence. Two cases of left atrial isomerism are reported here i...
Tracheobronchial compression by cardiovascular structures complicates the course after surgery of co...
Double outlet right ventricle associated with complete atrioventricular (AV) canal is a rare malform...
Right ventricle-dependent coronary circulation coexisting with left main coronary atresia in the set...
Surgical repair of aortic atresia with a large ventricular septal defect and a normally developed le...
AbstractThe cases of five patients with previous Senning ( n = 4) or Mustard ( n = 1) operations and...
A heart is described pathologically in which the aorta emerged from the right ven-tricle and was not...
The case of an infant with double outlet right ventricle with anatomically corrected malposition of ...
Biventricular repair in right atrial isomerism is rarely feasible due to associated anomalies of ven...
A 2 year old boy with ventricular inversion and normal ventriculoarterial connection is described. A...
Aortic atresia associated with ventriculoarterial discordance (transposition) was found at necropsy ...
Aortic atresia is rare in the setting of a normally developed left ventricle with a ventricular sept...
AbstractGross morphologic study of 14 hearts with congenitally corrected transposition or discordant...
A child presented at birth with severe cyanosis. Echocardiography showed hypoplasia of the right hea...
An isolated right superior vena cava (RSVC) draining into the left atrium represents a very rare con...
Atrial isomerism is very rare in adolescence. Two cases of left atrial isomerism are reported here i...
Tracheobronchial compression by cardiovascular structures complicates the course after surgery of co...
Double outlet right ventricle associated with complete atrioventricular (AV) canal is a rare malform...
Right ventricle-dependent coronary circulation coexisting with left main coronary atresia in the set...
Surgical repair of aortic atresia with a large ventricular septal defect and a normally developed le...
AbstractThe cases of five patients with previous Senning ( n = 4) or Mustard ( n = 1) operations and...
A heart is described pathologically in which the aorta emerged from the right ven-tricle and was not...
The case of an infant with double outlet right ventricle with anatomically corrected malposition of ...
Biventricular repair in right atrial isomerism is rarely feasible due to associated anomalies of ven...