一种罕见的复杂心脏异常

Journal of cardiology and cardiovascular medicine Pub Date : 2022-08-30 DOI:10.17352/2455-2976.000179

Kritika Kritika, Sharma Rajaram, Tiwari Tapendra, Goyal Saurabh

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摘要

先天性纠正性大动脉转位(TGA)是最罕见的复杂心脏异常之一，占先天性心脏病(CHD)的1%，占胎儿TGA的20%[1,2]。它的特征是房室不一致并伴有室动脉不一致。它的特征包括主动脉，起源于左侧形态的右心室，肺动脉的前部和左侧。

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A rare form of complex cardiac anomaly

Congenital corrected Transposition Of Great Arteries (TGA) is one of the rarest complex cardiac anomalies, comprising 1% of Congenital Heart Disease (CHD) and 20% of cases of fetal TGA [1,2]. It is characterized by an atrioventricular discordance with a concurrent ventricular-arterial discordance. Its features include the aorta, which arises from the left-sided morphologic right ventricle, anterior and left of the pulmonary artery.

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Journal of cardiology and cardiovascular medicine

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