• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[杜氏肌营养不良症中的完全性房室传导阻滞]

[Complete atrioventricular block in Duchenne muscular dystrophy].

作者信息

Kuru Satoshi, Tanahashi Tamotsu, Matsumoto Shinjirou, Kitamura Tetsuya, Konagaya Masaaki

机构信息

Department of Neurology, Suzuka National Hospital.

出版信息

Rinsho Shinkeigaku. 2012;52(9):685-7. doi: 10.5692/clinicalneurol.52.685.

DOI:10.5692/clinicalneurol.52.685
PMID:22989906
Abstract

We report a case of complete atrioventricular (AV) block in a 40-year-old patient with Duchenne muscular dystrophy (DMD). While he was bed-ridden and required mechanical ventilation, his cardiac involvement was mild. He had the deletion of exon 45-52 in the dystrophin gene. He underwent transient complete AV block and came to require pacemaker implantation due to recurrence of complete AV block ten days after the first attack. Electrophysiological study revealed mild prolonged AH and HV interval. Although DMD patients with AV block have been rarely reported so far, attention should be paid to AV block for patients who prolonged their lives.

摘要

我们报告了一例40岁的杜氏肌营养不良症(DMD)患者发生完全性房室传导阻滞的病例。当他卧床且需要机械通气时,其心脏受累情况较轻。他的肌营养不良蛋白基因存在外显子45 - 52缺失。他经历了短暂的完全性房室传导阻滞,并且在首次发作十天后因完全性房室传导阻滞复发而需要植入起搏器。电生理研究显示AH和HV间期轻度延长。尽管迄今为止很少有DMD患者发生房室传导阻滞的报道,但对于延长了生存期的患者,应关注房室传导阻滞。

相似文献

1
[Complete atrioventricular block in Duchenne muscular dystrophy].[杜氏肌营养不良症中的完全性房室传导阻滞]
Rinsho Shinkeigaku. 2012;52(9):685-7. doi: 10.5692/clinicalneurol.52.685.
2
Life-threatening Arrhythmias in a Becker Muscular Dystrophy Family due to the Duplication of Exons 3-4 of the Dystrophin Gene.由于肌营养不良蛋白基因外显子3-4重复导致的贝克型肌营养不良家族中的危及生命的心律失常。
Intern Med. 2015;54(23):3075-8. doi: 10.2169/internalmedicine.54.3986. Epub 2015 Dec 1.
3
[A case of pacemaker implantation for complete atrioventricular block associated with Duchenne muscular dystrophy].[一例与杜氏肌营养不良症相关的完全性房室传导阻滞的起搏器植入病例]
No To Hattatsu. 1997 Nov;29(6):476-80.
4
Complete atrioventricular block in Duchenne muscular dystrophy.杜氏肌营养不良症中的完全性房室传导阻滞。
Europace. 2008 Nov;10(11):1351-2. doi: 10.1093/europace/eun264. Epub 2008 Sep 24.
5
Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation.在两个患有严重智力障碍的杜氏肌营养不良症日本家庭中,发现由于肌营养不良蛋白基因的新突变导致第66外显子完全缺失。
Brain Dev. 2000 Mar;22(2):107-12. doi: 10.1016/s0387-7604(99)00126-6.
6
Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.杜兴氏和贝克氏肌肉营养不良症:一种分子与免疫组织化学方法
Arq Neuropsiquiatr. 2007 Mar;65(1):73-6. doi: 10.1590/s0004-282x2007000100016.
7
Duchenne muscular dystrophy in a female with compound heterozygous contiguous exon deletions.一名患有复合杂合性连续外显子缺失的女性的杜氏肌营养不良症。
Neuromuscul Disord. 2017 Jun;27(6):569-573. doi: 10.1016/j.nmd.2017.03.011. Epub 2017 Apr 3.
8
Complete atrioventricular block after isolated aortic valve replacement.单纯主动脉瓣置换术后发生完全性房室传导阻滞。
Kardiol Pol. 2016;74(9):985-93. doi: 10.5603/KP.a2016.0038. Epub 2016 Apr 4.
9
Baseline HV-interval predicts complete AV-block secondary to transcatheter aortic valve implantation.基线 HV 间期可预测经导管主动脉瓣植入术后继发的完全性房室传导阻滞。
Acta Cardiol. 2015 Oct;70(5):574-80. doi: 10.2143/AC.70.5.3110518.
10
Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community.在沙特社区的杜氏肌营养不良症患者中,对肌营养不良蛋白基因中外显子重排和移码的分子特征进行研究。
Hum Genomics. 2018 Apr 10;12(1):18. doi: 10.1186/s40246-018-0152-8.

引用本文的文献

1
Cardiac care of children with dystrophinopathy and females carrying DMD-gene variations.儿童肌营养不良症和携带 DMD 基因突变女性的心脏护理。
Open Heart. 2022 Oct;9(2). doi: 10.1136/openhrt-2022-001977.
2
Electrocardiographic features of children with Duchenne muscular dystrophy.Duchenne 型肌营养不良症患儿的心电图特征。
Orphanet J Rare Dis. 2022 Aug 20;17(1):320. doi: 10.1186/s13023-022-02473-9.
3
Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results.
对于终末期扩张型肌营养不良性心肌病患者植入心脏装置是否真的有益?文献综述及个人研究结果
Acta Myol. 2019 Mar 1;38(1):1-7. eCollection 2019 Mar.
4
Interventions for preventing and treating cardiac complications in Duchenne and Becker muscular dystrophy and X-linked dilated cardiomyopathy.杜氏和贝克型肌营养不良症以及X连锁扩张型心肌病中心脏并发症的预防和治疗干预措施。
Cochrane Database Syst Rev. 2018 Oct 16;10(10):CD009068. doi: 10.1002/14651858.CD009068.pub3.
5
Cardiac conduction disturbances and aging in patients with Duchenne muscular dystrophy.杜氏肌营养不良症患者的心脏传导障碍与衰老
Medicine (Baltimore). 2017 Oct;96(42):e8335. doi: 10.1097/MD.0000000000008335.
6
Treatment of dystrophin cardiomyopathies.肌营养不良性心肌病的治疗。
Nat Rev Cardiol. 2014 Mar;11(3):168-79. doi: 10.1038/nrcardio.2013.213. Epub 2014 Jan 14.