• 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

Hyperekplexia.

作者信息

Kurczynski T W

出版信息

Arch Neurol. 1983 Apr;40(4):246-8. doi: 10.1001/archneur.1983.04050040076015.

DOI:10.1001/archneur.1983.04050040076015
PMID:6830476
Abstract

Hyperekplexia is a hereditary neurologic disorder manifested by an exaggerated startle response, generalized muscular rigidity, and prominent nocturnal myoclonus. The distinctive features of this syndrome constitute an unusual clinical entity that is easily mistaken for other disorders. The study of a family provided additional data on various aspects of this condition. The proband was 3 months old when he was referred for persistent generalized stiffness since birth; this stiffness was associated with an exaggerated startle response and intermittent apnea. Similar symptoms in infancy and prominent nocturnal myoclonus with an excessive startle response in adulthood were described in other family members for five generations. Various features of the disorder indicate a relationship to the syndrome of the "jumping Frenchmen of Maine," latah, miryachit, and other unusual startle reactions.

摘要

相似文献

1
Hyperekplexia.
Arch Neurol. 1983 Apr;40(4):246-8. doi: 10.1001/archneur.1983.04050040076015.
2
[Hyperekplexia -- a treatable neuropediatric disease].[僵人综合征——一种可治疗的神经儿科疾病]
Klin Padiatr. 2005 Jul-Aug;217(4):220-1. doi: 10.1055/s-2004-820286.
3
[Startle disease: growing rigid with fear].[惊吓症:因恐惧而变得僵硬]
Ned Tijdschr Geneeskd. 1995 Sep 23;139(38):1940-3.
4
Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutations.由于GLRA1基因突变的复合杂合性导致的惊跳症表型。
Ann Neurol. 1999 Oct;46(4):634-8. doi: 10.1002/1531-8249(199910)46:4<634::aid-ana12>3.0.co;2-9.
5
Hyperekplexia-like syndromes without mutations in the GLRA1 gene.GLRA1基因无突变的类惊跳症综合征
Clin Neurol Neurosurg. 1997 Aug;99(3):172-8. doi: 10.1016/s0303-8467(97)00022-x.
6
Hyperekplexia and stiff-baby syndrome: an identical neurological disorder?惊跳症与僵人综合征:一种相同的神经系统疾病?
Ital J Neurol Sci. 1993 Mar;14(2):145-52. doi: 10.1007/BF02335749.
7
Hyperekplexia: pedigree studies in two families.
Am J Med Genet. 1991 Aug 1;40(2):138-43. doi: 10.1002/ajmg.1320400203.
8
Hyperekplexia and sudden neonatal death.
Pediatr Neurol. 1992 May-Jun;8(3):221-5. doi: 10.1016/0887-8994(92)90073-8.
9
Exaggerated startle reactions.夸张的惊跳反应。
Clin Neurophysiol. 2012 Jan;123(1):34-44. doi: 10.1016/j.clinph.2011.09.022. Epub 2011 Oct 26.
10
Hyperekplexia in neonates.新生儿的惊吓症
Postgrad Med J. 2001 Sep;77(911):570-2. doi: 10.1136/pmj.77.911.570.

引用本文的文献

1
Abnormal neurodevelopment outcome in case of neonatal hyperekplexia secondary to missense mutation in gene.基因错义突变继发新生儿惊吓症时的异常神经发育结局
BMJ Case Rep. 2020 Dec 15;13(12):e236152. doi: 10.1136/bcr-2020-236152.
2
Glycine receptor mouse mutants: model systems for human hyperekplexia.甘氨酸受体小鼠突变体:人类惊跳症的模型系统。
Br J Pharmacol. 2013 Nov;170(5):933-52. doi: 10.1111/bph.12335.
3
A novel syndrome of lethal familial hyperekplexia associated with brain malformation.一种与脑畸形相关的致死性家族性肌阵挛新型综合征。
BMC Neurol. 2012 Oct 27;12:125. doi: 10.1186/1471-2377-12-125.
4
The glycinergic system in human startle disease: a genetic screening approach.人类惊吓病中的甘氨酸能系统:一种遗传筛查方法。
Front Mol Neurosci. 2010 Mar 23;3:8. doi: 10.3389/fnmol.2010.00008. eCollection 2010.
5
Movement disorder emergencies.运动障碍急症
J Neurol. 2008 Aug;255 Suppl 4:2-13. doi: 10.1007/s00415-008-4002-9.
6
Glycinergic and GABA(A)-mediated inhibition of somatic motoneurons does not mediate rapid eye movement sleep motor atonia.甘氨酸能和γ-氨基丁酸A(GABA(A))介导的对躯体运动神经元的抑制并不介导快速眼动睡眠运动无张力。
J Neurosci. 2008 Apr 2;28(14):3535-45. doi: 10.1523/JNEUROSCI.5023-07.2008.
7
Movement disorder emergencies.运动障碍急症
Curr Neurol Neurosci Rep. 2005 Jul;5(4):284-93. doi: 10.1007/s11910-005-0073-5.
8
Hyperekplexia in neonates.新生儿的惊吓症
Postgrad Med J. 2001 Sep;77(911):570-2. doi: 10.1136/pmj.77.911.570.
9
Transient neuromotor phenotype in transgenic spastic mice expressing low levels of glycine receptor beta-subunit: an animal model of startle disease.表达低水平甘氨酸受体β亚基的转基因痉挛小鼠的短暂神经运动表型:惊吓疾病的动物模型
Eur J Neurosci. 2000 Jan;12(1):27-32. doi: 10.1046/j.1460-9568.2000.00877.x.
10
Properties of human glycine receptors containing the hyperekplexia mutation alpha1(K276E), expressed in Xenopus oocytes.在非洲爪蟾卵母细胞中表达的含有惊跳症突变α1(K276E)的人类甘氨酸受体的特性。
J Physiol. 1998 Feb 15;507 ( Pt 1)(Pt 1):25-40. doi: 10.1111/j.1469-7793.1998.025bu.x.