• 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

[青少年帕金森病的诊断与治疗进展]

[Progress in diagnosis and treatment of juvenile parkinsonism].

作者信息

Ishikawa A

机构信息

Department of Neurology, Nishiojiya National Sanatorium.

出版信息

Nihon Rinsho. 1993 Nov;51(11):2947-51.

PMID:7903987
Abstract

The diagnosis and treatment of juvenile parkinsonism (JP) is described. There was a high incidence of familial JP (58.1%), and its inheritance pattern was usually an autosomal recessive type. The patients with JP presented with improvement of parkinsonian symptoms following sleep and dystonic posture of the feet as specific signs. The tremor was a fine postural, and impairment of postural reflex was prominent. In the treatment of JP, it is important to control the wearing-off phenomenon and the dopa-induced choreic dyskinesia usually occurring in the extremities. A small dose of levodopa with decarboxylase inhibitor has to be carefully administered several times a day. The clinical course of JP is very slowly progressive compared with that of Parkinson's disease.

摘要

本文描述了青少年帕金森病(JP)的诊断与治疗。家族性JP的发病率较高(58.1%),其遗传模式通常为常染色体隐性遗传型。JP患者表现出睡眠后帕金森症状改善以及足部肌张力障碍姿势等特异性体征。震颤为精细姿势性震颤,姿势反射障碍较为突出。在JP的治疗中,控制通常出现在四肢的剂末现象和多巴诱导的舞蹈症异动症很重要。必须谨慎地每天多次给予小剂量左旋多巴与脱羧酶抑制剂。与帕金森病相比,JP的临床病程进展非常缓慢。

相似文献

1
[Progress in diagnosis and treatment of juvenile parkinsonism].[青少年帕金森病的诊断与治疗进展]
Nihon Rinsho. 1993 Nov;51(11):2947-51.
2
[Clinical characteristics and linkage analysis of autosomal recessive form of juvenile parkinsonism(AR-JP)].青少年帕金森病常染色体隐性遗传型(AR-JP)的临床特征及连锁分析
Nihon Rinsho. 1997 Jan;55(1):83-8.
3
[Treatment and prognosis of juvenile parkinsonism--L-dopa responsiveness].青少年帕金森病的治疗与预后——左旋多巴反应性
Nihon Rinsho. 1997 Jan;55(1):101-5.
4
[A 62-year-old man with familial parkinsonism with the onset at 24 years of the age].一名62岁男性,患有家族性帕金森病,发病于24岁。
No To Shinkei. 1996 Jun;48(6):587-97.
5
[Autosomal recessive early-onset parkinsonism with diurnal fluctuation (AR-EPDF)--clinical characteristics].[常染色体隐性早发型帕金森病伴日间波动(AR-EPDF)——临床特征]
Rinsho Shinkeigaku. 1996 Aug;36(8):944-50.
6
Young-onset Parkinson's disease revisited--clinical features, natural history, and mortality.再探早发型帕金森病——临床特征、自然史及死亡率
Mov Disord. 1998 Nov;13(6):885-94. doi: 10.1002/mds.870130605.
7
Clinical and neuropathological aspects of autosomal recessive juvenile parkinsonism.常染色体隐性少年型帕金森病的临床与神经病理学特征
J Neurol. 1998 Nov;245(11 Suppl 3):P4-9. doi: 10.1007/pl00007745.
8
[A case of autosomal recessive juvenile parkinsonism (AR-JP) with onset at the age of 6 years].一例6岁起病的常染色体隐性遗传性少年帕金森病(AR-JP)
Rinsho Shinkeigaku. 2000 Jun;40(6):596-9.
9
A family with hereditary juvenile dystonia-parkinsonism.一个患有遗传性青少年肌张力障碍-帕金森综合征的家族。
Mov Disord. 1995 Jul;10(4):482-8. doi: 10.1002/mds.870100413.
10
[Benefit of L-DOPA-without-DCI (decarboxylase inhibitor) therapy on wearing-off phenomenon in advanced stages of Parkinson's disease patients].左旋多巴无脱羧酶抑制剂疗法对帕金森病患者晚期剂末现象的益处
No To Shinkei. 2002 Feb;54(2):127-32.