The history of Jervell and Lange-Nielsen syndrome.

IF 1.2 Q2 MEDICINE, GENERAL & INTERNAL
Tidsskrift for Den Norske Laegeforening Pub Date : 2024-12-16 Print Date: 2024-12-17 DOI:10.4045/tidsskr.24.0412
Erlend Hem, Knut Tjøl Gjesdal, Lisbeth Tranebjærg, Magne Nylenna
{"title":"The history of Jervell and Lange-Nielsen syndrome.","authors":"Erlend Hem, Knut Tjøl Gjesdal, Lisbeth Tranebjærg, Magne Nylenna","doi":"10.4045/tidsskr.24.0412","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>First-time documentation of rare diseases is normally in the form of case reports. These are typically based on unexpected observations by vigilant clinicians and lead to further research on prevalence and aetiology. One of the best-known Norwegian examples is Jervell and Lange-Nielsen syndrome.</p><p><strong>Material and method: </strong>We conducted a literature review using systematic database searches and historical analysis.</p><p><strong>Results and interpretation: </strong>The Norwegian internal medicine specialists Anton Jervell (1901-87) and Fred Lange-Nielsen (1919-89) published an article in 1957 in the American Heart Journal describing a Norwegian family in which four of the six children were deaf and experienced recurrent syncope. Three of the children died suddenly. This rare condition was the first evidence of prolonged QT intervals on an ECG as a risk factor for sudden cardiac death.</p>","PeriodicalId":23123,"journal":{"name":"Tidsskrift for Den Norske Laegeforening","volume":"144 15","pages":""},"PeriodicalIF":1.2000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tidsskrift for Den Norske Laegeforening","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4045/tidsskr.24.0412","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/17 0:00:00","PubModel":"Print","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

Background: First-time documentation of rare diseases is normally in the form of case reports. These are typically based on unexpected observations by vigilant clinicians and lead to further research on prevalence and aetiology. One of the best-known Norwegian examples is Jervell and Lange-Nielsen syndrome.

Material and method: We conducted a literature review using systematic database searches and historical analysis.

Results and interpretation: The Norwegian internal medicine specialists Anton Jervell (1901-87) and Fred Lange-Nielsen (1919-89) published an article in 1957 in the American Heart Journal describing a Norwegian family in which four of the six children were deaf and experienced recurrent syncope. Three of the children died suddenly. This rare condition was the first evidence of prolonged QT intervals on an ECG as a risk factor for sudden cardiac death.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Tidsskrift for Den Norske Laegeforening
Tidsskrift for Den Norske Laegeforening MEDICINE, GENERAL & INTERNAL-
CiteScore
0.60
自引率
18.20%
发文量
593
审稿时长
28 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信