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

研究成果: Article › 査読

30 被引用数 (Scopus)

抄録

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).

本文言語	English
ページ（範囲）	70-72
ページ数	3
ジャーナル	Pediatric Cardiology
巻	24
号	1
DOI	https://doi.org/10.1007/s00246-002-0169-5
出版ステータス	Published - 2003 1月
外部発表	はい

ASJC Scopus subject areas

小児科学、周産期医学および子どもの健康
循環器および心血管医学

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10.1007/s00246-002-0169-5

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AU - Miura, M.

AU - Yamagishi, H.

AU - Morikawa, Y.

AU - Matsuoka, R.

PY - 2003/1

Y1 - 2003/1

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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EP - 72

JO - Pediatric Cardiology

JF - Pediatric Cardiology

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

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