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遗传性长 QT 综合征

籍振国 马国平

实用心电学杂志2016,Vol.25Issue(5):305-308,4.
实用心电学杂志2016,Vol.25Issue(5):305-308,4.DOI:10.13308/j.issn.2095-9354.2016.05.001

遗传性长 QT 综合征

Congenital long-QT syndrome

籍振国 1马国平1

作者信息

  • 1. 050031 河北 石家庄,河北医科大学第一医院心内科
  • 折叠

摘要

Abstract

This paper mainly discusses the different manifestations,clinical diagnosis and treat-ment of commonly seen congenital long-QT syndrome.The past two decades has witnessed dramatic changes of its treatment.This paper gives a brief introduction to its risk stratification and screening of suspected patients,and also provides suggestions for young athletes with LQTS.For the cases with a medical history of syncope or convulsion,especially with a family history of inexplicable sudden death among first-degree relatives,LQTS-related examination and diagnosis should be recommen-ded.The treatment for congenital LQTS includes changes of life style,and rational drug and non-drug therapies.

关键词

遗传性/长QT综合征/遗传学/尖端扭转型室性心动过速

Key words

heredity/long-QT syndrome/genetics/torsades de pointes

分类

医药卫生

引用本文复制引用

籍振国,马国平..遗传性长 QT 综合征[J].实用心电学杂志,2016,25(5):305-308,4.

实用心电学杂志

2095-9354

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