دوره 8، شماره 2 - ( 1-1399 )                   جلد 8 شماره 2 صفحات 7-7 | برگشت به فهرست نسخه ها

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Ghaemi H R, Zamani H, Babazadeh K, Navaeifar M R. Anomalous origin of left coronary artery from pulmonary artery (ALCAPA): a case series and review of literature. J. Pediatr. Rev. 2020; 8 (2) :7-7
URL: http://jpr.mazums.ac.ir/article-1-246-fa.html
Anomalous origin of left coronary artery from pulmonary artery (ALCAPA): a case series and review of literature. Journal of Pediatrics Review. 1399; 8 (2) :7-7

URL: http://jpr.mazums.ac.ir/article-1-246-fa.html


چکیده:   (570 مشاهده)
Introduction: Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare Cardiovascular Disease presented with an incidence of 1:300000 live births.
Case Presentation: In this manuscript, four cases of ALCAPA in infancy were described. Two infants were presented with respiratory distress and two with heart a murmur. Their coronary artery was derived from the pulmonary artery. Two of them died, one after surgical procedure and one before surgical intervention. Of remained cases, one of them had a good surgical outcome and another was missed in follow up.
A brief review was done on case reports of ALCAPA in children. Eighteen manuscripts were found including 201 pediatric cases.
Conclusions: The vast majority of affected children will die within the first year of life if ALCAPA is not diagnosed and treated correctly.
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نوع مطالعه: Case Report and Review of Literature |
دریافت: 1398/3/26 | پذیرش: 1398/6/16 | انتشار: 1398/10/9

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