• 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

患有杜氏肌营养不良症的男性有阅读障碍的风险吗?

Are males with Duchenne muscular dystrophy at risk for reading disabilities?

作者信息

Hendriksen Jos G M, Vles Johan S H

机构信息

Childhood Rehabilitation Centre Franciscusoord, Stichting Revalidatie Limburg, Valkenburg a/d Geul, The Netherlands.

出版信息

Pediatr Neurol. 2006 Apr;34(4):296-300. doi: 10.1016/j.pediatrneurol.2005.08.029.

DOI:10.1016/j.pediatrneurol.2005.08.029
PMID:16638505
Abstract

Males with Duchenne muscular dystrophy have sub-average cognitive capacities and may manifest more specifically language-related deficits. In the current study, the information-processing capacity, reading performance, and behavioral functioning of 25 Dutch males with Duchenne muscular dystrophy (mean age 10.1 years) were systematically assessed. This study relied on the use of a new battery of tests to explore more precisely reading disabilities in males with Duchenne muscular dystrophy. Five of the males had serious reading problems and another five had moderate reading problems, which indicates that reading problems are significantly more common in males with Duchenne muscular dystrophy than in males from a normal population. These reading problems were independent of the level of information processing and behavioral functioning. Implications of these findings and possible directions for future research are discussed, especially with regard to the early detection and treatment of reading problems in males with Duchenne muscular dystrophy.

摘要

患有杜氏肌营养不良症的男性认知能力低于平均水平,可能更具体地表现出与语言相关的缺陷。在当前研究中,对25名患有杜氏肌营养不良症的荷兰男性(平均年龄10.1岁)的信息处理能力、阅读表现和行为功能进行了系统评估。本研究依靠使用一套新的测试来更精确地探究患有杜氏肌营养不良症男性的阅读障碍。其中五名男性存在严重阅读问题,另外五名存在中度阅读问题,这表明阅读问题在患有杜氏肌营养不良症的男性中比在正常人群的男性中明显更常见。这些阅读问题与信息处理水平和行为功能无关。讨论了这些发现的意义以及未来研究的可能方向,特别是关于患有杜氏肌营养不良症男性阅读问题的早期检测和治疗。

相似文献

1
Are males with Duchenne muscular dystrophy at risk for reading disabilities?患有杜氏肌营养不良症的男性有阅读障碍的风险吗?
Pediatr Neurol. 2006 Apr;34(4):296-300. doi: 10.1016/j.pediatrneurol.2005.08.029.
2
Cognitive and psychological profile of males with Becker muscular dystrophy.贝克型肌营养不良男性患者的认知和心理特征
J Child Neurol. 2008 Feb;23(2):155-62. doi: 10.1177/0883073807307975. Epub 2007 Dec 3.
3
Neuropsychiatric disorders in males with duchenne muscular dystrophy: frequency rate of attention-deficit hyperactivity disorder (ADHD), autism spectrum disorder, and obsessive--compulsive disorder.杜氏肌营养不良男性患者的神经精神障碍:注意缺陷多动障碍(ADHD)、自闭症谱系障碍和强迫症的发病率
J Child Neurol. 2008 May;23(5):477-81. doi: 10.1177/0883073807309775. Epub 2008 Mar 19.
4
Intellectual and behavioral functioning in a South african cohort of boys with duchenne muscular dystrophy.南非杜兴氏肌肉营养不良男孩队列中的智力和行为功能
J Child Neurol. 2011 Aug;26(8):963-9. doi: 10.1177/0883073811399149. Epub 2011 Apr 27.
5
Depression in parents of children with Duchenne muscular dystrophy.杜氏肌营养不良症患儿父母的抑郁情绪。
Pediatr Neurol. 2004 Jul;31(1):16-9. doi: 10.1016/j.pediatrneurol.2004.01.011.
6
Quality of life in Duchenne muscular dystrophy: the subjective impact on children and parents.杜氏肌营养不良症患者的生活质量:对儿童及其父母的主观影响
J Child Neurol. 2011 Jun;26(6):707-13. doi: 10.1177/0883073810389043. Epub 2011 Apr 11.
7
Reading impairment in Duchenne muscular dystrophy: A pilot study to investigate similarities and differences with developmental dyslexia.杜氏肌营养不良症中的阅读障碍:一项调查其与发育性阅读障碍异同的试点研究。
Res Dev Disabil. 2015 Oct-Nov;45-46:168-77. doi: 10.1016/j.ridd.2015.07.025. Epub 2015 Aug 6.
8
Duchenne muscular dystrophy: issues in expanding newborn screening.杜氏肌营养不良症:扩大新生儿筛查中的问题
Curr Opin Pediatr. 2007 Dec;19(6):700-4. doi: 10.1097/MOP.0b013e3282f19f65.
9
[Psychological characteristics of children suffering from Duchenne muscular dystrophy].[杜兴氏肌营养不良症患儿的心理特征]
Przegl Lek. 2002;59(10):811-4.
10
Psychosocial adjustment in males with Duchenne muscular dystrophy: psychometric properties and clinical utility of a parent-report questionnaire.杜氏肌营养不良男性患者的心理社会适应:一份家长报告问卷的心理测量特性及临床效用
J Pediatr Psychol. 2009 Jan-Feb;34(1):69-78. doi: 10.1093/jpepsy/jsn067. Epub 2008 Jul 22.

引用本文的文献

1
Understanding Duchenne muscular dystrophy-associated brain pathology.了解杜兴氏肌营养不良症相关的脑部病理。
Dis Model Mech. 2025 Jul 1;18(7). doi: 10.1242/dmm.052302. Epub 2025 Aug 1.
2
Duchenne muscular dystrophy: recent insights in brain related comorbidities.杜氏肌营养不良症:脑相关合并症的最新见解
Nat Commun. 2025 Feb 3;16(1):1298. doi: 10.1038/s41467-025-56644-w.
3
Reading skills over time among children with Duchenne muscular dystrophy.杜兴氏肌肉营养不良症患儿的阅读技能随时间的变化情况。
Child Neuropsychol. 2025 Apr;31(3):467-486. doi: 10.1080/09297049.2024.2386078. Epub 2024 Aug 1.
4
Duchenne muscular dystrophy: disease mechanism and therapeutic strategies.杜氏肌营养不良症:疾病机制与治疗策略。
Front Physiol. 2023 Jun 26;14:1183101. doi: 10.3389/fphys.2023.1183101. eCollection 2023.
5
Wechsler Scale Intelligence Testing in Males with Dystrophinopathies: A Review and Meta-Analysis.肌营养不良男性患者的韦氏智力量表智力测试:综述与荟萃分析
Brain Sci. 2022 Nov 14;12(11):1544. doi: 10.3390/brainsci12111544.
6
Development of a novel startle response task in Duchenne muscular dystrophy.开发一种新的杜氏肌营养不良症惊跳反应任务。
PLoS One. 2022 Apr 19;17(4):e0264091. doi: 10.1371/journal.pone.0264091. eCollection 2022.
7
Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study.神经肌肉疾病影响数字表征与处理:一项探索性研究。
Front Psychol. 2021 Sep 6;12:697881. doi: 10.3389/fpsyg.2021.697881. eCollection 2021.
8
Cognitive Deficits in Myopathies.肌肉病的认知缺陷。
Int J Mol Sci. 2020 May 27;21(11):3795. doi: 10.3390/ijms21113795.
9
Cognitive impairment appears progressive in the mdx mouse.mdx 小鼠的认知障碍似乎呈进行性发展。
Neuromuscul Disord. 2020 May;30(5):368-388. doi: 10.1016/j.nmd.2020.02.018. Epub 2020 Mar 4.
10
Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy.抗肌萎缩蛋白 Dp71 与杜氏肌营养不良症的神经发病机制。
Mol Neurobiol. 2020 Mar;57(3):1748-1767. doi: 10.1007/s12035-019-01845-w. Epub 2019 Dec 13.