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Anomalous origin of the left coronary artery from the pulmonary artery: A midterm experience of a rare entity at a tertiary care center

ALCAPA is a rare congenital heart disease. Presentation varies from asymptomatic to progressive heart failure and death. Surgical repair is indicated in all patients with a goal of restoring two coronary systems. Data was analysed in regard to presenting features, echocardiographic findings, various...

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Hlavní autoři: Rahul Bhushan, Manish Mallik, Ketika Potey, Vijay Grover, Palash Aiyer, Narender S. Jhajhria
Médium: Artigo
Jazyk:Inglês
Vydáno: Tabriz University of Medical Sciences 2023-09-01
Edice:Journal of Cardiovascular and Thoracic Research
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On-line přístup:https://jcvtr.tbzmed.ac.ir/PDF/jcvtr-15-181.pdf
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