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Article

[Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 1 Dec 2009

Shi Rui-ming, Ma Ai-qun, Zhang Yan-min, Yang Chun, Huang Chen, Zhou Xi-hui, Liu Xiao-hong

Abstract excerpt

OBJECTIVE: The congenital long QT syndrome (LQTs) is a hereditary disorder in which most affected family members have delayed ventricular repolarization manifested on the electrocardiogram (ECG) as QT interval prolongation. The disorder is associated with an increased propensity to arrhythmogenic syncope, polymorphous ventricular tachycardia (torsade de pointes), and sudden arrhythmic death. LQTs is due to...

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Source

Identifiers

PMID: 20193146

Genes

KCNH2
KCNQ1

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