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一名患有唐氏综合征和完全性房室通道缺损的13岁患者出现QT间期延长。

Prolonged QT in a 13-year-old patient with Down syndrome and complete atrioventricular canal defect.

作者信息

Tisma-Dupanovic Svjetlana, Gowdamarajan Rengasamy, Goldenberg Ilan, Huang David T, Knilans Timothy, Towbin Jeffrey A

机构信息

School of Medicine, Kansas City, University of Missouri-Kansas City, MO, USA.

出版信息

Ann Noninvasive Electrocardiol. 2011 Oct;16(4):403-6. doi: 10.1111/j.1542-474X.2011.00471.x.

DOI:10.1111/j.1542-474X.2011.00471.x
PMID:22008496
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6932648/
Abstract

Ann Noninvasive Electrocardiol 2011;16(4):403–406

摘要

《无创心电图学杂志》2011年；第16卷第4期：403 - 406页

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本文引用的文献

1
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.携带KCNJ2基因突变的安德森-陶威尔综合征患者的心电图特征：特征性T-U波形态可预测KCNJ2基因型。
Circulation. 2005 May 31;111(21):2720-6. doi: 10.1161/CIRCULATIONAHA.104.472498. Epub 2005 May 23.
2
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).与LQT7（安德森综合征）相关的KCNJ2突变的功能和临床特征
J Clin Invest. 2002 Aug;110(3):381-8. doi: 10.1172/JCI15183.
3
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome.Kir2.1基因的突变导致安德森综合征的发育性和发作性电表型。
Cell. 2001 May 18;105(4):511-9. doi: 10.1016/s0092-8674(01)00342-7.