• 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

[进行性杜氏肌营养不良症的诊断特征]

[Characteristics of the diagnosis of progressive Duchenne muscular dystrophy].

作者信息

Temin P A, Zavadenko N N, Kamennykh L N, Nikanorova M Iu

出版信息

Zh Nevropatol Psikhiatr Im S S Korsakova. 1989;89(3):93-6.

PMID:2728756
Abstract

A total of 70 patients with Duchenne progressive muscular dystrophy (DPMD) aged 3 to 20 were enrolled in this study. Peculiarities of the diagnosis and diagnostic errors were shown at different stages of medical follow-up of the patients. A half of the patients had pediatrists and orthopedists as their first doctors. Upon the initial investigation, DPMD was diagnosed in about 1/3 of the patients. Retarded motor and psycholingual development were the first signs of the disease in 72.9% and 37.1% of the cases, respectively. Bones and cartilages were also frequently changed. To improve the early DPMD diagnosis it is essential that pediatrists child surgeons and ortopedists be largely informed about the clinical features of the disease.

摘要

本研究共纳入70例年龄在3至20岁的杜氏进行性肌营养不良(DPMD)患者。研究显示了患者医疗随访不同阶段的诊断特点及诊断错误情况。一半患者首诊医生为儿科医生和骨科医生。初步检查时,约1/3的患者被诊断为DPMD。运动发育迟缓及精神语言发育迟缓分别是72.9%和37.1%病例的首发症状。骨骼和软骨也常有改变。为改善DPMD的早期诊断,儿科医生、儿童外科医生和骨科医生必须充分了解该疾病的临床特征。

相似文献

1
[Characteristics of the diagnosis of progressive Duchenne muscular dystrophy].[进行性杜氏肌营养不良症的诊断特征]
Zh Nevropatol Psikhiatr Im S S Korsakova. 1989;89(3):93-6.
2
[Differential diagnosis of Becker and Duchenne muscular dystrophy].[贝克肌营养不良症和杜氏肌营养不良症的鉴别诊断]
Gac Med Mex. 1994 Nov-Dec;130(6):454-8.
3
[Delayed diagnosis of Duchenne muscular dystrophy in Chile].[智利杜兴氏肌营养不良症的延迟诊断]
Rev Med Chil. 1999 Jan;127(1):65-70.
4
[Relations between delayed diagnosis and forms of onset in Duchenne muscular dystrophy].[杜氏肌营养不良症中延迟诊断与发病形式之间的关系]
Gac Med Mex. 1994 Nov-Dec;130(6):459-64.
5
[Progressive Duchenne muscular dystrophy: general practice aspects of diagnostic assessment].[进行性杜氏肌营养不良症:诊断评估的全科医学方面]
Monatsschr Kinderheilkd. 1987 Jun;135(6):320-4.
6
[Errors in the diagnosis of progressive muscular dystrophy and spinal muscular atrophy].
Z Arztl Fortbild (Jena). 1981 Jul 1;75(13):577-81.
7
[A diagnostic algorithm--infantile hypotonia (the "flabby" child)].一种诊断算法——婴儿肌张力减退(“松软”儿童)
Pediatrie (Bucur). 1992 Apr-Jun;41(2):85-90.
8
Clinico-morphological correlative aspects in progressive muscular dystrophy.进行性肌营养不良的临床形态学相关方面
Morphol Embryol (Bucur). 1984 Apr-Jun;30(2):123-8.
9
Comparative analysis between Duchenne and Becker types muscular dystrophy.杜兴氏和贝克氏型肌营养不良症的比较分析
Electromyogr Clin Neurophysiol. 1999 Jul-Aug;39(5):315-8.
10
Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood.某些神经源性肌病以及某些在婴儿期和儿童早期导致肌肉无力、肌张力减退和萎缩的肌源性肌病的特征性临床发现。
Birth Defects Orig Artic Ser. 1971 Feb;7(2):72-81.