Anomalous origin of Left Coronary Artery from Pulmonary Artery; Congenital Anomaly Presenting with Dyspnea. A rare Case Study

Journal Title: Medical Science and Discovery - Year 2015, Vol 2, Issue 6

Abstract

Anomalous origin of left coronary artery from pulmonary artery (ALCAPA) is rare congenital anomaly. Most of these patients die is infancy. Presentation in adulthood is very rare. Clinical manifestation in teenagers or young adult contains arrhythmia, myocardial perfusion likely causes significant chest pain and these symptoms of myocardial ischemia may be misinterpreted as routine infantile colic and sudden death.

Authors and Affiliations

Shahriar Anvari, Sohrab Negargar, Ahmad Jamei Khosroshahi

Keywords

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  • EP ID EP520433
  • DOI -
  • Views 32
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How To Cite

Shahriar Anvari, Sohrab Negargar, Ahmad Jamei Khosroshahi (2015). Anomalous origin of Left Coronary Artery from Pulmonary Artery; Congenital Anomaly Presenting with Dyspnea. A rare Case Study. Medical Science and Discovery, 2(6), 358-61. https://europub.co.uk./articles/-A-520433