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

M. Miura; H. Yamagishi; Y. Morikawa; R. Matsuoka

doi:10.1007/s00246-002-0169-5

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

M. Miura, H. Yamagishi, Y. Morikawa, R. Matsuoka

Department of Pediatrics

Research output: Contribution to journal › Article › peer-review

29 Citations (Scopus)

Abstract

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).

Original language	English
Pages (from-to)	70-72
Number of pages	3
Journal	Pediatric Cardiology
Volume	24
Issue number	1
DOIs	https://doi.org/10.1007/s00246-002-0169-5
Publication status	Published - 2003 Jan 1

Keywords

2:1 atrioventricular block
Infant
LQT3
Long QT syndrome

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Cardiology and Cardiovascular Medicine

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10.1007/s00246-002-0169-5

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abstract = "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).",

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AU - Matsuoka, R.

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N2 - 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).

AB - 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).

KW - 2:1 atrioventricular block

KW - Infant

KW - LQT3

KW - Long QT syndrome

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

Abstract

Keywords

ASJC Scopus subject areas

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