Congenital long QT syndrome and 2:1 atrioventricular block with a mutation of the SCN5A gene

被引：22
|
作者：
Miura, M
Yamagishi, H
Morikawa, Y
Matsuoka, R
机构：
[1] Keio Univ Hosp, Dept Pediat, Shinjuku Ku, Tokyo 1608582, Japan
[2] Tokyo Womens Med Coll, Inst Heart, Dept Pediat Cardiol, Tokyo, Japan
来源：
PEDIATRIC CARDIOLOGY | 2003年 / 24卷 / 01期
关键词：
long QT syndrome; 2 : 1 atrioventricular block; infant; LQT3;
D O I：
10.1007/s00246-002-0169-5
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Infants with congenital long QT syndrome (LQTS) and 2:1 atrioventricular block (AVB) have been recognized as a clinical subset of children with LQTS. However, the genotype of this disorder is not well-known. We report an infant with LQTS and 2:1 AVB with a mutation of the SCN5A gene (LQT3). In some patients with LQTS and 2:1 AVB, the disorder may be due to mutation of the SCN5A gene (LQT3).
引用
收藏
页码：70 / 72
页数：3
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