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Truncus arteriosus communis in combination with cor triatriatum sinsitrum
Elmar Klusmeier1, Nikolaus A Haas1, Eugen Sandica2
11Department for Pediatric Cardiology/Congenital Heart Defects,Centre for Congenital Heart Defects,Heart and Diabetes Centre North-Rhine Westfalia,Germany.
Cardiology in the Young
|May 1, 2015
Summary
This case study reports the first known instance of truncus arteriosus communis and cor triatriatum sinistrum coexisting. Successful surgical intervention was achieved for this rare congenital heart defect combination.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Truncus arteriosus communis (TAC) is a rare congenital heart defect (CHD) comprising 1% of all cardiac abnormalities.
- TAC often presents with other cardiac malformations, including truncal valve and aortic arch abnormalities.
- Cor triatriatum sinistrum (CTS) is another rare CHD, frequently associated with other cardiac defects.
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