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Published on: July 18, 2014
Congenitally corrected transposition of the great arteries
Seon-Hye Kim1,2, Mamoru Tanaka3, Momo Umezu3
1Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan. kim-sh@kmh.gr.jp.
Insights
Congenitally corrected transposition of the great arteries (cTGA) is a rare heart defect. This case highlights prenatal diagnosis of cTGA using specific imaging views, even without other cardiac anomalies.
Area of Science:
- Cardiology
- Medical Imaging
- Fetal Medicine
Background:
- Congenitally corrected transposition of the great arteries (cTGA) is an uncommon congenital heart malformation.
- cTGA involves discordant atrioventricular and ventriculoarterial connections, often with associated anomalies.
- Prenatal detection of cTGA can be challenging due to subtle presentations and mimicry of other conditions like complete TGA.
Purpose of the Study:
- To report a case of in utero diagnosis of cTGA.
- To emphasize the diagnostic utility of specific echocardiographic views for cTGA.
- To highlight the importance of identifying cTGA prenatally, even in the absence of other cardiac defects.
Main Methods:
- Fetal echocardiography at 29 weeks' gestation.
- Detailed examination of the four-chamber view to assess atrioventricular connections.
- Assessment of the spatial relationship of the great vessels.
Main Results:
- A diagnosis of cTGA was made prenatally at 29 weeks' gestation.
- No additional cardiac anomalies were identified prenatally.
- Postnatal findings included a patent ductus arteriosus with bidirectional flow.
Conclusions:
- Accurate prenatal diagnosis of cTGA is possible with careful echocardiographic assessment.
- Identifying atrioventricular discordance and the parallel course of great vessels (l-transposition) are key.
- Early prenatal diagnosis of cTGA facilitates timely postnatal management.
Abstract:
Congenitally corrected transposition of the great arteries (cTGA) is an uncommon cardiac malformation characterized by discordant atrioventricular and ventriculoarterial connections. Most cases of cTGA are associated with cardiac anomalies. As the ventricular outflow tract may appear to arise correctly from the right and left ventricles, cases of cTGA with a mild associated anomaly are rarely detected prenatally. Parallel vessels are evident in cTGA, but this sign is also present in complete TGA. We report a case of cTGA diagnosed in utero at 29 weeks' gestation. The fetus was diagnosed as TGA and referred to our hospital at 28 weeks' gestation. cTGA was found at 29 weeks' gestation in our hospital, and no additional cardiac anomalies were seen prenatally. After birth, patent ductus arteriosus with bidirectional flow was present. Careful examination of the four-chamber view suggested atrioventricular discordance. Identification of a parallel course of the great vessels, with the aorta anterior and to the left of the pulmonary trunk (l-transposition), may help accurate prenatal diagnosis of cTGA.
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