• 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

[Congenital myopathy without specific features (minimal change myopathy)].

作者信息

Shen D G

出版信息

Zhonghua Shen Jing Jing Shen Ke Za Zhi. 1989 Feb;22(1):39-40, 63.

PMID:2805977
Abstract

A case of Congenital myopathy without specific features was reported. The main clinical findings were generalized muscle weakness and delayed developmental milestones. Histological and histochemical examination on the biopsied muscles demonstrated minimal nonspecific changes, mild variation in fiber size without structure and enzyme abnormality. No prominent necrotic changes were found and Ulrich and Fukuyama type of congenital myopathy were excluded. The abnormal muscle pathology was assumed to have resulted from delayed muscle fiber growth due to defective neural influence.

摘要

相似文献

1
[Congenital myopathy without specific features (minimal change myopathy)].
Zhonghua Shen Jing Jing Shen Ke Za Zhi. 1989 Feb;22(1):39-40, 63.
2
Congenital myopathy without specific features (minimal change myopathy).无特异性表现的先天性肌病（微小病变性肌病）
Neuropediatrics. 1983 Nov;14(4):237-41. doi: 10.1055/s-2008-1059586.
3
Fiber density in congenital muscle fiber type disproportion. II. Congenital muscle hypotonia and hip dislocation.
Electromyogr Clin Neurophysiol. 1991 Jan-Feb;31(1):5-8.
4
Clinical and histologic changes in the follow-up of a congenital myopathy.
Pediatr Neurol. 2005 Aug;33(2):139-41. doi: 10.1016/j.pediatrneurol.2005.02.012.
5
Fetal muscle characteristics in nemaline myopathy.
Neuropediatrics. 1983 Feb;14(1):47-52. doi: 10.1055/s-2008-1059552.
6
Congenital myopathy with type 2A muscle fiber uniformity and smallness.
Neuropediatrics. 1992 Feb;23(1):10-3. doi: 10.1055/s-2008-1071303.
7
[Neonatal hypotonia of muscular origin: analysis of 50 cases].[肌肉源性新生儿肌张力低下：50例分析]
Neurologia. 2001 Jun-Jul;16(6):245-53.
8
Congenital familial myopathy with type 2 fiber hypoplasia and type 1 fiber predominance.
Brain Dev. 1997 Jul;19(5):362-5. doi: 10.1016/s0387-7604(97)00036-3.
9
Congenital fiber type disproportion: a rare type of congenital myopathy: a report of four cases.先天性纤维类型不均衡：一种罕见的先天性肌病：4例报告
Neurol India. 2004 Jun;52(2):254-6.
10
Congenital fiber type disproportion in identical twins.
Ann Neurol. 1977 Dec;2(6):455-9. doi: 10.1002/ana.410020603.