Karacaglar Emir, Aydinalp Alp, Coskun Mehmet, Muderrisoglu Haldun
Cardiology Department;
Radiodiagnostic, Baskent University School of Medicine, Bahcelievler/Ankara, Turkey.
Clin Pract. 2011 Dec 5;1(4):e85. doi: 10.4081/cp.2011.e85. eCollection 2011 Sep 28.
Anomalous origin of coronary arteries is also a relatively rare congenital malformation and has been reported as the cause of angina pectoris and arrhythmia. Long QT syndrome (LQTS) is a rare inherited arrythmogenic disease characterized by susceptibility to life-threatening arrhytmias andsudden cardiac death. We present a 36-year-old patient in whom two rare anomalies coexist and treated succesfully with β-blocker therapy.
冠状动脉异常起源也是一种相对罕见的先天性畸形，已被报道为心绞痛和心律失常的病因。长QT综合征（LQTS）是一种罕见的遗传性致心律失常疾病，其特征是易发生危及生命的心律失常和心源性猝死。我们报告一名36岁患者，其同时存在两种罕见异常，并通过β受体阻滞剂治疗成功治愈。
