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The diagnosis and treatment of cardiac ion channelopathies: congenital long QT syndrome and Brugada syndrome.

作者信息

Aleong Ryan G, Milan David J, Ellinor Patrick T

机构信息

Cardiac Arrhythmia Service and Cardiovascular Research Center, Massachusetts General Hospital, 55 Fruit Street, GRB 109, Boston, MA 02114, USA.

出版信息

Curr Treat Options Cardiovasc Med. 2007 Oct;9(5):364-71. doi: 10.1007/s11936-007-0056-8.

DOI:10.1007/s11936-007-0056-8
PMID:17897565
Abstract

Sudden cardiac death in young adults can be due to a range of conditions including coronary disease, hypertrophic or dilated cardiomyopathy, and arrhythmogenic right ventricular cardiomyopathy. Although each of these disorders has typical pathologic findings, some victims display no overt abnormalities and are presumed to have died from a primary cardiac arrhythmia. Increasingly, these malignant arrhythmias have been demonstrated to be due to mutations in ion channels. In this review we focus on the two most common of these disorders, termed ion channelopathies, namely congenital long QT syndrome and Brugada syndrome.

摘要

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JAMA. 2006 Sep 13;296(10):1249-54. doi: 10.1001/jama.296.10.1249.
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ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines (writing committee to develop Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death): developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society.美国心脏病学会/美国心脏协会/欧洲心脏病学会2006年室性心律失常患者管理和心源性猝死预防指南:美国心脏病学会/美国心脏协会特别工作组和欧洲心脏病学会实践指南委员会(制定室性心律失常患者管理和心源性猝死预防指南的写作委员会)报告:与欧洲心律协会和心律协会合作制定。
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