Congenital Long QT Syndrome Associated with Localization-related Epilepsy: Interictal Electroencephalogram Abnormalities Detected after the Second Syncope
Author:
Affiliation:
1. Department of Pediatrics, Hirosaki National Hospital
2. Department of Pediatrics, Hirosaki University School of Medicine
Publisher
The Japanese Society of Pediatric Cardiology and Cardiac Surgery
Subject
Polymers and Plastics,General Environmental Science
Link
https://www.jstage.jst.go.jp/article/jspccs/32/4/32_2016-0013/_pdf
Reference10 articles.
1. 1) Ballardie FW, Murphy RP, Davis J: Epilepsy: A presentation of the Romano–Ward syndrome. Br Med J (Clin Res Ed) 1983; 287: 896–897
2. 2) MacCormick JM, McAlister H, Crawford J, et al: Misdiagnosis of long QT syndrome as epilepsy at first presentation. Ann Emerg Med 2009; 54: 26–32
3. 5) Priori SG, Schwartz PJ, Napolitano C, et al: Risk stratification in the long-QT syndrome. N Engl J Med 2003; 348: 1866–1874
4. 6) Shimizu W, Horie M, Ohno S, et al: Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome. Multicenter study in Japan. J Am Coll Cardiol 2004; 44: 117–125
5. 7) Barsheshet A, Goldenberg I, O-Uchi J, et al: Mutation in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events. Implications for mutation-specific response to β-blocker therpy in type1 long-QT syndrome. Circulation 2012; 125: 1988–1996
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