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

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

Research output: Contribution to journalArticle

26 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 languageEnglish
Pages (from-to)70-72
Number of pages3
JournalPediatric Cardiology
Volume24
Issue number1
DOIs
Publication statusPublished - 2003 Jan

Fingerprint

Romano-Ward Syndrome
Atrioventricular Block
Mutation
Genes
Long QT Syndrome
Genotype

Keywords

  • 2:1 atrioventricular block
  • Infant
  • Long QT syndrome
  • LQT3

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Pediatrics, Perinatology, and Child Health

Cite this

Congenital long QT syndrome and 2 : 1 atrioventricular block with a mutation of the SCN5A gene. / Miura, M.; Yamagishi, Hiroyuki; Morikawa, Y.; Matsuoka, R.

In: Pediatric Cardiology, Vol. 24, No. 1, 01.2003, p. 70-72.

Research output: Contribution to journalArticle

@article{d2b29e0ffe6d41fb83f13ca06d796e84,
title = "Congenital long QT syndrome and 2: 1 atrioventricular block with a mutation of the SCN5A gene",
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).",
keywords = "2:1 atrioventricular block, Infant, Long QT syndrome, LQT3",
author = "M. Miura and Hiroyuki Yamagishi and Y. Morikawa and R. Matsuoka",
year = "2003",
month = "1",
doi = "10.1007/s00246-002-0169-5",
language = "English",
volume = "24",
pages = "70--72",
journal = "Pediatric Cardiology",
issn = "0172-0643",
publisher = "Springer New York",
number = "1",

}

TY - JOUR

T1 - Congenital long QT syndrome and 2

T2 - 1 atrioventricular block with a mutation of the SCN5A gene

AU - Miura, M.

AU - Yamagishi, Hiroyuki

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 - Long QT syndrome

KW - LQT3

UR - http://www.scopus.com/inward/record.url?scp=0037645439&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0037645439&partnerID=8YFLogxK

U2 - 10.1007/s00246-002-0169-5

DO - 10.1007/s00246-002-0169-5

M3 - Article

C2 - 12574983

AN - SCOPUS:0037645439

VL - 24

SP - 70

EP - 72

JO - Pediatric Cardiology

JF - Pediatric Cardiology

SN - 0172-0643

IS - 1

ER -