Scimitar syndrome associated with complete transposition of the great arteries
نویسندگان
چکیده
منابع مشابه
Hypoplastic 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 کاملAortic 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 کاملTransposition of the great arteries
Transposition of the great arteries (TGA), also referred to as complete transposition, is a congenital cardiac malformation characterised by atrioventricular concordance and ventriculoarterial (VA) discordance. The incidence is estimated at 1 in 3,500-5,000 live births, with a male-to-female ratio 1.5 to 3.2:1. In 50% of cases, the VA discordance is an isolated finding. In 10% of cases, TGA is ...
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ژورنال
عنوان ژورنال: European Heart Journal
سال: 2013
ISSN: 1522-9645,0195-668X
DOI: 10.1093/eurheartj/eht145