Coarctation of the aorta in the syndrome of absent pulmonary valve with ventricular septal defect

1990 ◽  
Vol 11 (3) ◽  
pp. 159-163 ◽  
Author(s):  
Michael Hofbeck ◽  
Georg Röckelein ◽  
Helmut Singer ◽  
Jochen Rein ◽  
Adriana C. Gittenberger-de Groot
1974 ◽  
Vol 8 (4) ◽  
pp. 355-355 ◽  
Author(s):  
Jane L Todd ◽  
Ellis L Jones ◽  
Dorothy E Brinsfield ◽  
William H Plauth ◽  
Richard W Blumberg

2019 ◽  
Vol 10 (4) ◽  
pp. 513-514
Author(s):  
Ashish Katewa ◽  
Nishith Bhargava ◽  
Balswaroop Sahu ◽  
Atul Prabhu ◽  
Shivani Gajpal

Absent pulmonary valve is a rare congenital heart defect where the pulmonary valve is either absent or rudimentary. It is usually associated with tetralogy of Fallot although it has been reported with other lesions. We present a rare case of absent pulmonary valve associated with transposition of great arteries and non-routable ventricular septal defect that was surgically managed by aortic root translocation.


1994 ◽  
Vol 4 (2) ◽  
pp. 184-186 ◽  
Author(s):  
Dennis Kececioglu ◽  
Omar Galal ◽  
Fuad Abbag

SummaryA rare association of ‘absent pulmonary valve’ syndrome, midmuscular ventricular septal defect and aneurysmatic dilation of the ascending aorta without pathology of the aortic valve is described in a 10-month-old infant. The diagnosis was established by echocardiography and angiography.


1990 ◽  
Vol 66 (2) ◽  
pp. 233-234 ◽  
Author(s):  
Jose A. Ettedgui ◽  
Gurleen K. Sharland ◽  
Sunder K. Chita ◽  
Andrew Cook ◽  
Nuala Fagg ◽  
...  

Author(s):  
Nick Archer ◽  
Nicky Manning

This chapter explores right-sided abnormalities, discussing the venoatrial junction (including both azygous/hemiazygous connections and abnormal systemic venous drainage), the atrioventricular junction (including tricuspid atresia and Ebstein’s anomaly/tricuspid valve dysplasia), and the ventriculoarterial junction (including pulmonary stenosis, pulmonary atresia with intact septum, tetralogy of Fallot, tetralogy of Fallot with absent pulmonary valve, pulmonary atresia with ventricular septal defect, and double outlet right ventricle), and arterial abnormalities.


2016 ◽  
Vol 9 (1) ◽  
pp. 101-104 ◽  
Author(s):  
Ayano Futuki ◽  
Keiichi Fujiwara ◽  
Kosuke Yoshizawa ◽  
Hisanori Sakazaki

Of the associated cardiac defects with absent pulmonary valve, the combination of tricuspid atresia, ventricular septal defect, and aneurysmal dilatation of the pulmonary arteries is very rare. We report the case of a low-birth-weight girl (2,282 g) with this anomaly, which was prenatally diagnosed. Fontan completion was successfully achieved at 16 months of age, following staged palliative procedures including banding of the main pulmonary trunk and plication of the aneurysmal dilated central pulmonary artery.


2004 ◽  
Vol 14 (4) ◽  
pp. 402-408 ◽  
Author(s):  
Nili Zucker ◽  
Ilya Rozin ◽  
Aviva Levitas ◽  
Eli Zalzstein

So-called ‘absent pulmonary valve syndrome’ is a rare cardiac malformation, usually associated with tetralogy of Fallot. Congenital absence of the leaflets of the pulmonary valve is less common when the ventricular septum is intact. Characteristic features of the syndrome include dysplasia or absence of the pulmonary valvar leaflets, permitting severe pulmonary regurgitation, and aneurysmal dilation of the pulmonary arteries. The purpose of our study was to review our experience with patients diagnosed as having the absent pulmonary valve syndrome, and to describe their clinical presentation, natural history, and outcome. We reviewed retrospectively data from 18 patients with absent pulmonary valve syndrome, 10 boys and eight girls, treated between March 1983 and May 2003. We identified two groups of patients, one made up of 11 patients with a ventricular septal defect, in whom the morphology of the subpulmonary outflow tract was phenotypic for tetralogy of Fallot, and another group, with seven patients, having an intact ventricular septum. Family history of congenital heart disease was common only in patients with ventricular septal defect, being found in 73%, all of whom were diagnosed during infancy with variable respiratory distress. Diagnosis was delayed in 43% of the patients with an intact ventricular septum. Cardiac surgery was performed in eight patients with ventricular septal defect (73%), compared to only two patients (28%) with an intact ventricular septum. Overall mortality was 28%, with five patients dying. Although our sample was small, two clinical patterns emerged depending on the presence or absence of a ventricular septal defect. Patients with a ventricular septal defect and phenotypic features of tetralogy of Fallot have a strong family history of congenital cardiac disease, develop respiratory symptoms during infancy and exhibit a variable prognosis, despite cardiac surgery. Patients with an intact ventricular septum are usually asymptomatic, present later in life, and show a relatively benign prognosis.


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