• 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

[采用标点量表对强直性肌营养不良(斯坦纳特病)患者进行口腔面部评估]

[Orofacial evaluation with a punctuation scale in patients with myotonic dystrophy (Steinert's disease)].

作者信息

Noronha C F, Alves Duro L A

机构信息

Instituto de Neurologia Deolindo Couto (INDC), Universidade Federal do Rio de Janeiro (UFRJ), Brasil.

出版信息

Arq Neuropsiquiatr. 1995 Sep;53(3-A):424-31.

PMID:8540816
Abstract

Orofacial examination was applied in 39 patients with myotonic dystrophy. We made an original table with a scale of punctuation. The group showed a deficit of 43.70%. The female group was 6.16% better than male's. The maternal inherited cases were 3.63% better than the paternal ones. When we separated the groups by decades, there was a tendency to an increasingly better performance as the age of the beggining of symptoms was later. The performance was 10.68% better in the group of patients with 1 to 10 years than in the group with 11 to 20 years of disease. We concluded that the phonoaudiological affection in myotonic dystrophy was less intense in patients with later onset of symptoms and less than 10 years of disease.

摘要

对39例强直性肌营养不良患者进行了口面部检查。我们制作了一个带有评分量表的原始表格。该组显示出43.70%的缺陷。女性组比男性组好6.16%。母系遗传病例比父系遗传病例好3.63%。当我们按十年划分组时,随着症状开始年龄越晚,表现有越来越好的趋势。发病1至10年的患者组比发病11至20年的患者组表现好10.68%。我们得出结论,强直性肌营养不良患者中,症状出现较晚且患病时间少于10年的患者,其听觉语音障碍程度较轻。

相似文献

1
[Orofacial evaluation with a punctuation scale in patients with myotonic dystrophy (Steinert's disease)].[采用标点量表对强直性肌营养不良(斯坦纳特病)患者进行口腔面部评估]
Arq Neuropsiquiatr. 1995 Sep;53(3-A):424-31.
2
[Myotonic dystrophy severity (Steinert's disease) (author's transl)].强直性肌营养不良严重程度(斯坦纳特病)(作者译)
Sem Hop. 1980;56(7-8):335-40.
3
[Maxillofacial manifestations of Steinert's myotonic dystrophy. Clinical and therapeutic aspects].[斯坦纳特肌强直性营养不良的颌面表现。临床与治疗方面]
Rev Stomatol Chir Maxillofac. 1995;96(2):74-82.
4
[The stomatological complications of Steinert's disease. Apropos of a case].[斯坦纳特病的口腔并发症。关于一例病例]
Rev Stomatol Chir Maxillofac. 1984;85(1):28-33.
5
The expanding clinical and genetic spectrum of the myotonic dystrophies.强直性肌营养不良症不断扩展的临床和基因谱。
Acta Neurol Belg. 2000 Sep;100(3):151-5.
6
[Steinert's myotonic dystrophy and Thomsen's congenital myotonia. Observation of a family (author's transl)].[斯坦纳特型强直性肌营养不良症与汤姆森先天性肌强直。一个家族的观察(作者译)]
Riv Patol Nerv Ment. 1979 Jul-Aug;100(4):209-19.
7
[Clinical manifestations of myotonic dystrophy: epidemiologic survey].[强直性肌营养不良的临床表现:流行病学调查]
Med Clin (Barc). 1993 Jun 26;101(5):161-4.
8
[Steinert's disease and pregnancy. A case report and recent literature].[施泰纳特病与妊娠。一例病例报告及近期文献]
J Gynecol Obstet Biol Reprod (Paris). 1995;24(2):177-80.
9
[Conventional and quantitative electroencephalography in patients with Steinert's myotonic dystrophy].[斯坦纳特型强直性肌营养不良患者的传统脑电图和定量脑电图]
Rev Neurol. 2004;39(1):12-7.
10
Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions.1型强直性肌营养不良症患者小CTG重复扩增的临床特征
Neurology. 2006 Apr 25;66(8):1248-50. doi: 10.1212/01.wnl.0000208513.48550.08.