Successful total correction of congenital interruption of the aortic arch and ventricular septal defect.
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چکیده
منابع مشابه
Interrupted aortic arch in a child with trisomy 5q31.1q35.1 due to a maternal (20;5) balanced insertion.
Complex congenital heart defects (CHD) are associated with a variety of single gene abnormalities and chromosomal rearrangements. Of the various forms of CHD, aortic arch interruption, a conotruncal heart defect, is relatively uncommon. Here we report a male neonate with aortic arch interruption type B, secundum atrial septal defect, perimembranous ventricular septal defect, patent ductus arter...
متن کاملInterrupted right aortic arch in DiGeorge syndrome.
The clinical and necropsy findings in four cases of interrupted right aortic arch and right descending aorta associated with DiGeorge syndrome (congenital absence or hypoplasia of the thymus and parathyroids) are described. All patients had a mirror image of type B interruption, namely a right aortic arch with reversed branching pattern and an interruption between the right common carotid and r...
متن کاملInterruption of the aortic arch.
Interruption of the aortic arch is an uncommon malformation in which there is no direct continuity between the aortic arch and the descending aorta, the latter arising through a patent ductus arteriosus. Three types are described, depending upon the site of interruption in relation to the arch vessels. A large ventricular septal defect is present in 94% of cases. It is to be distinguished from ...
متن کاملInterruption of aortic arch without associated cardiac abnormalities.
Interruption of the aortic arch is an infrequent congenital anomaly. In its usual variety it is almost constantly associated with a persistent ductus arteriosus which provides adequate blood flow to the descending aorta. Coincidental cardiac malformations are often present, such as a ventricular septal defect or a bicuspid aortic valve, among many others. Isolated absence or interruption of the...
متن کامل[Aortopulmonary window: clinical assessment and surgical results].
INTRODUCTION AND OBJECTIVES Aortopulmonary septal defect is an uncommon congenital cardiac anomaly. To date, approximately 300 cases have been reported. We present our experience, emphasizing the importance of early correction to avoid irreversible pulmonary hypertension. PATIENTS AND METHOD Between 1979 and 2000, seven patients underwent surgical repair of this heart defect in our hospital. ...
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عنوان ژورنال:
- Thorax
دوره 25 5 شماره
صفحات -
تاریخ انتشار 1970