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Frequency of abnormal electroencephalogram in asymptomatic relatives of patients with epilepsy: A systematic review and meta-analaysis

机译:无症状的癫痫患者亲属中异常脑电图的频率:系统评价和荟萃分析

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摘要

Objective: To systematically review studies of asymptomatic relatives of patients with Juvenile Myoclonic (JME), Childhood Absence (CAE) and Benign Rolandic (RE) Epilepsy who had an abnormal electroencephalogram (EEG) recording and determine the frequency of these waves through meta-analysis in order to better understand the genetics and mode of inheritance of idiopathic epilepsy.;Methods: MEDLINE, EMBASE, CINHAL and Cochrane databases were searched. Two independent reviewers conducted all screening levels, data abstraction, and quality appraisal. A meta-analysis was performed.;Results: After screening 10,233 citations and 211 full-text articles, 15 studies were included. A total 3885 asymptomatic relatives were included. The prevalence of all abnormal waves in asymptomatic relatives was 31%. Prevalence for each epilepsy type was 21% for JME, 42% for CAE and 33% for RE.;Conclusion: Further investigations are needed to test inheritance patterns to identify "major" genes.
机译:目的:系统地回顾脑电图(EEG)异常记录的幼年肌阵挛(JME),儿童缺席(CAE)和良性罗兰迪奇(RE)癫痫患者无症状亲属的研究,并通过荟萃分析确定这些波动的频率为了更好地了解特发性癫痫的遗传学和遗传模式。方法:检索MEDLINE,EMBASE,CINHAL和Cochrane数据库。两名独立的评审人员进行了所有筛选级别,数据抽象和质量评估。结果:筛选了10,233篇文献和211篇全文后,纳入15篇研究。包括3885名无症状亲属。无症状亲属中所有异常波的患病率为31%。对于JME,每种癫痫类型的患病率为21%,对于CAE为42%,对于RE为33%。结论:需要进一步的研究以测试遗传模式以鉴定“主要”基因。

著录项

  • 作者

    Tashkandi, Mariam.;

  • 作者单位

    University of Toronto (Canada).;

  • 授予单位 University of Toronto (Canada).;
  • 学科 Epidemiology.;Genetics.;Neurosciences.
  • 学位 M.Sc.
  • 年度 2016
  • 页码 174 p.
  • 总页数 174
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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