Complete transposition of great arteries with coarctation of aorta.
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چکیده
منابع مشابه
Aortic atresia occurring with complete transposition of great arteries.
Aortic atresia occurring with complete transposition of the great arteries (ventriculoarterial discordance) has not previously been reported. A patient with this condition is described, who is alive and relatively well at the age of 6 years. This survival contrasts conspicuously with that of patients with the far commoner situation of aortic atresia with normally connected great arteries. It is...
متن کاملHypoplastic left heart with complete transposition of the great arteries.
A male newborn infant with hypoplastic left heart and transposition of the great arteries died on the second day of life. The haemodynamic consequences of this malformation are considerably different from those of ordinary hypoplastic left heart syndrome because of pulmonary rather than aortic atresia. In the absence of cross sectional echocardiographic equipment, cardiac catheterisation with a...
متن کاملA 33-day-old Infant with the Transposition of the Great Arteries; A Rare Case Report
Dextro-transposition of the great arteries (d-TGA) is the one most common cyanotic congenital heart disease in neonates. The discordant ventriculoarterial arrangement results in parallel circulation, it so is vital to understand the management. We report a rare interesting but critical case of 33-day-old boy who developed cyanosis and had transposition of great arteries combined with interrupte...
متن کاملCoarctation of aorta with complete aortic occlusion
Survival to advanced age is exceptional in patients with unrepaired aortic coarctation. We report the case of an 81-year-old man with aortic coarctation and total occlusion who was otherwise asymptomatic. Coarctation was suspected when a femoral-radial pulse delay was noted during his routine physical examination. A 70-mmHg systolic blood pressure gradient between the upper and lower extremitie...
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ژورنال
عنوان ژورنال: Heart
سال: 1982
ISSN: 1355-6037
DOI: 10.1136/hrt.48.6.566