• 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

散发性舞蹈病的持久之谜:单中心病例系列。

The enduring enigma of sporadic chorea: A single center case series.

机构信息

Department of Neurology, Fundacion Jimenez Diaz, Madrid, Spain.

Department of Genetics, Fundacion Jimenez Diaz, Madrid, Spain.

出版信息

Tremor Other Hyperkinet Mov (N Y). 2023 Sep 7;13:33. doi: 10.5334/tohm.800. eCollection 2023.

DOI:10.5334/tohm.800
PMID:37692071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10487123/
Abstract

UNLABELLED

Chorea can have a wide variety of causes including neurodegenerative, pharmacological, structural, metabolic, infectious, immunologic and paraneoplastic processes. We reviewed the clinical records of patients with apparently sporadic choreic movements and no relevant family history, who presented to our neurology department (Hospital Fundación Jimenez Diaz) between 1991 and 2022. We detected 38 cases of apparent sporadic chorea (ASC); Our analysis revealed 5 cases of genetic chorea (including 3 cases with Huntington's disease) while 6 cases were autoimmune/hematological; 6 drug-related chorea, 5 metabolic-vascular, 5 due to miscellaneous conditions and 4 were of mixed etiology. No clear etiology was identified in 8 cases. The differential diagnosis of ASC is extensive and challenging.

HIGHLIGHTS

Chorea can have a wide variety of genetic and sporadic causesWe reviewed the clinical records of patients with apparently sporadic chorea (ASC), who presented to our neurology department over the last 30 yearsWe detected 38 cases of apparent ASC; Our analysis revealed a wide array of different sporadic conditions and 5 cases of genetic choreaThe differential diagnosis of ASC is extensive and challenging.

摘要

未注明

舞蹈症有多种原因,包括神经退行性、药物性、结构性、代谢性、感染性、免疫性和副肿瘤性过程。我们回顾了 1991 年至 2022 年期间在我们神经内科(Hospital Fundación Jimenez Diaz)就诊的、有明显散发性舞蹈运动且无相关家族史的患者的临床记录。我们共发现 38 例明显散发性舞蹈症(ASC);分析显示 5 例为遗传性舞蹈症(包括 3 例亨廷顿病),6 例为自身免疫/血液系统疾病;6 例与药物相关,5 例为代谢-血管性,5 例为其他原因,4 例为混合病因。8 例病因不明确。ASC 的鉴别诊断广泛且具有挑战性。

要点

舞蹈症有多种遗传性和散发性病因。我们回顾了过去 30 年来在我们神经内科就诊的、有明显散发性舞蹈症(ASC)的患者的临床记录。我们共发现 38 例明显 ASC;分析显示,有多种不同的散发性疾病,以及 5 例遗传性舞蹈症。ASC 的鉴别诊断广泛且具有挑战性。

相似文献

1
The enduring enigma of sporadic chorea: A single center case series.散发性舞蹈病的持久之谜:单中心病例系列。
Tremor Other Hyperkinet Mov (N Y). 2023 Sep 7;13:33. doi: 10.5334/tohm.800. eCollection 2023.
2
Cause and course in a series of patients with sporadic chorea.一系列散发性舞蹈病患者的病因及病程
J Neurol. 2003 Apr;250(4):429-35. doi: 10.1007/s00415-003-1010-7.
3
Huntington's disease and other choreas.亨廷顿舞蹈症及其他舞蹈病。
J Neurol. 1998 Nov;245(11):709-16. doi: 10.1007/s004150050272.
4
Hereditary chorea - what else to consider when the Huntington's disease genetics test is negative?遗传性舞蹈病——当亨廷顿舞蹈症基因检测呈阴性时还需考虑哪些因素?
Acta Neurol Scand. 2017 Jan;135(1):25-33. doi: 10.1111/ane.12609. Epub 2016 May 6.
5
[Differential diagnosis of chorea].[舞蹈病的鉴别诊断]
Brain Nerve. 2009 Aug;61(8):963-71.
6
Chorea in the Elderly: A Differential Diagnosis and Case Report of Late-Onset Huntington's Disease in an Octogenarian.老年人舞蹈症:一例八旬晚发性亨廷顿病的鉴别诊断及病例报告。
J Huntingtons Dis. 2023;12(4):377-380. doi: 10.3233/JHD-230596.
7
The causes of sporadic and 'senile' chorea.散发性和“老年性”舞蹈病的病因。
Aust N Z J Med. 1998 Aug;28(4):429-31. doi: 10.1111/j.1445-5994.1998.tb02075.x.
8
Huntington disease and Huntington disease-like in a case series from Brazil.巴西病例系列中的亨廷顿病和亨廷顿病样疾病。
Clin Genet. 2014 Oct;86(4):373-7. doi: 10.1111/cge.12283. Epub 2013 Oct 17.
9
Huntington disease and other choreas.亨廷顿舞蹈症及其他舞蹈病。
Neurol Clin. 2009 Aug;27(3):719-36, vi. doi: 10.1016/j.ncl.2009.04.001.
10
Late onset levodopa responsive Huntington's disease with minimal chorea masquerading as Parkinson plus syndrome.迟发性左旋多巴反应性亨廷顿舞蹈病,伴轻微舞蹈症,伪装成帕金森叠加综合征。
J Neurol Neurosurg Psychiatry. 2000 Feb;68(2):238-41. doi: 10.1136/jnnp.68.2.238.

本文引用的文献

1
Disorders of Movement due to Acquired and Traumatic Brain Injury.后天性和创伤性脑损伤所致的运动障碍
Curr Phys Med Rehabil Rep. 2022;10(4):311-323. doi: 10.1007/s40141-022-00368-1. Epub 2022 Sep 22.
2
Treatable Hyperkinetic Movement Disorders Not to Be Missed.不可漏诊的可治疗性运动亢进性疾病
Front Neurol. 2021 Dec 1;12:659805. doi: 10.3389/fneur.2021.659805. eCollection 2021.
3
A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors.一项关于风湿性舞蹈病的全国性研究:临床特征、治疗和预后因素。
Eur J Paediatr Neurol. 2022 Jan;36:1-6. doi: 10.1016/j.ejpn.2021.11.002. Epub 2021 Nov 6.
4
Uremic Striatopallidal Syndrome Manifesting as Acute Onset Chorea.表现为急性起病舞蹈症的尿毒症性纹状体苍白球综合征
Mov Disord Clin Pract. 2021 Sep 3;8(Suppl 1):S55-S57. doi: 10.1002/mdc3.13285. eCollection 2021 Aug.
5
Adult-onset sporadic chorea: real-world data from a single-centre retrospective study.成人发作散发性舞蹈病:单中心回顾性研究的真实世界数据。
Neurol Sci. 2022 Jan;43(1):387-392. doi: 10.1007/s10072-021-05332-w. Epub 2021 May 26.
6
The extrapyramidal syndromes of chronic kidney disease and dialysis (EPS-CKDD): diagnostic criteria, risk factors and prognosis.慢性肾脏病和透析相关的锥体外系综合征(EPS-CKDD):诊断标准、危险因素和预后。
QJM. 2022 Jun 7;115(6):359-366. doi: 10.1093/qjmed/hcab140.
7
Expanding the Spectrum of Movement Disorders Associated With Hexanucleotide Expansions.扩展与六核苷酸重复扩增相关的运动障碍谱。
Neurol Genet. 2021 Mar 12;7(2):e575. doi: 10.1212/NXG.0000000000000575. eCollection 2021 Apr.
8
Case report and literature review of Huntington disease with intermediate CAG expansion.亨廷顿病伴中等程度CAG重复序列扩增的病例报告及文献综述
BMJ Neurol Open. 2020 Feb 9;2(1):e000027. doi: 10.1136/bmjno-2019-000027. eCollection 2020.
9
Movement Disorders and Hematologic Diseases.运动障碍与血液系统疾病
Mov Disord Clin Pract. 2020 Dec 29;8(2):193-207. doi: 10.1002/mdc3.13129. eCollection 2021 Feb.
10
Hemichorea as Presentation of Acute Cortical Ischemic Stroke. Case Series and Review of the Literature.以偏侧舞蹈症为表现的急性皮质性脑梗死。病例系列及文献复习。
J Stroke Cerebrovasc Dis. 2020 Oct;29(10):105150. doi: 10.1016/j.jstrokecerebrovasdis.2020.105150. Epub 2020 Jul 27.