• 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

相似文献

1
Men with an FMR1 premutation and their health education needs.携带 FMR1 前突变的男性及其健康教育需求。
J Genet Couns. 2021 Aug;30(4):1156-1167. doi: 10.1002/jgc4.1399. Epub 2021 Mar 31.
2
Improving Health Education for Women Who Carry an FMR1 Premutation.改善对携带FMR1前突变女性的健康教育。
J Genet Couns. 2016 Apr;25(2):228-38. doi: 10.1007/s10897-015-9862-4. Epub 2015 Jul 16.
3
Static and dynamic postural control deficits in aging fragile X mental retardation 1 (FMR1) gene premutation carriers.衰老脆性 X 智力低下 1 型 (FMR1) 基因前突变携带者的静态和动态姿势控制缺陷。
J Neurodev Disord. 2019 Jan 21;11(1):2. doi: 10.1186/s11689-018-9261-x.
4
Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.脆性 X 相关震颤/共济失调综合征:FMR1 基因对正常和前突变等位基因男性运动纤维束的影响。
JAMA Neurol. 2013 Aug;70(8):1022-9. doi: 10.1001/jamaneurol.2013.2934.
5
An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS).脆性 X 智力低下 1 基因前突变携带者在执行工作记忆任务时的前额叶活动的 fMRI 研究,包括伴有和不伴有脆性 X 相关震颤共济失调综合征(FXTAS)的患者。
J Psychiatr Res. 2011 Jan;45(1):36-43. doi: 10.1016/j.jpsychires.2010.04.030. Epub 2010 May 31.
6
Characterization and Early Detection of Balance Deficits in Fragile X Premutation Carriers With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS).伴有和不伴有脆性X相关震颤/共济失调综合征(FXTAS)的脆性X前突变携带者平衡缺陷的特征与早期检测
Cerebellum. 2015 Dec;14(6):650-62. doi: 10.1007/s12311-015-0659-7.
7
Altered expression of the FMR1 splicing variants landscape in premutation carriers.脆性 X 智力低下 1 号基因剪接变异体景观在前突变携带者中的改变表达。
Biochim Biophys Acta Gene Regul Mech. 2017 Nov;1860(11):1117-1126. doi: 10.1016/j.bbagrm.2017.08.007. Epub 2017 Sep 7.
8
FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening.西班牙共济失调患者中的脆性X震颤共济失调综合征:支持对女性FMR1前突变进行筛查。
Mol Neurobiol. 2007 Jun;35(3):324-8. doi: 10.1007/s12035-007-0020-3.
9
Screening for the FMR1 premutation in Greek patients with late-onset movement disorders.对希腊晚发性运动障碍患者中 FMR1 前突变的筛查。
Parkinsonism Relat Disord. 2023 Feb;107:105253. doi: 10.1016/j.parkreldis.2022.105253. Epub 2022 Dec 20.
10
Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Pathophysiology and Clinical Implications.脆性 X 相关震颤/共济失调综合征(FXTAS):发病机制与临床意义。
Int J Mol Sci. 2020 Jun 20;21(12):4391. doi: 10.3390/ijms21124391.

引用本文的文献

1
Experiences and perceptions of Chinese patients enrolled in a clinical trial assessing tuina and manual therapies for knee osteoarthritis: a nested qualitative study.参加评估推拿和手法治疗膝骨关节炎的临床试验的中国患者的体验与认知:一项嵌套式定性研究
BMC Complement Med Ther. 2025 May 28;25(1):191. doi: 10.1186/s12906-025-04926-7.
2
A scoping review of health literacy in rare disorders: key issues and research directions.罕见病健康素养的范围综述:关键问题和研究方向。
Orphanet J Rare Dis. 2024 Sep 6;19(1):328. doi: 10.1186/s13023-024-03332-5.

本文引用的文献

1
Health knowledge of women with a fragile X premutation: Improving understanding with targeted educational material.脆性 X 前突变妇女的健康知识:用有针对性的教育材料提高理解。
J Genet Couns. 2020 Dec;29(6):983-991. doi: 10.1002/jgc4.1222. Epub 2020 Jan 30.
2
Fragile X-Associated Tremor/Ataxia Syndrome: Unmet Needs and a Path for the Future.脆性X相关震颤/共济失调综合征:未满足的需求与未来之路
Front Genet. 2018 Jun 7;9:100. doi: 10.3389/fgene.2018.00100. eCollection 2018.
3
'Who is going to explain it to me so that I understand?' Health care needs and experiences of older patients with advanced heart failure.“谁能给我解释一下,好让我明白呢?”老年晚期心力衰竭患者的医疗保健需求与经历。
Eur J Ageing. 2012 Sep 22;9(4):297-303. doi: 10.1007/s10433-012-0244-6. eCollection 2012 Dec.
4
"It was a lot Tougher than I Thought It would be". A Qualitative Study on the Changing Nature of Being a Hemophilia Carrier.“这比我想象的要难得多”。一项关于血友病携带者身份变化本质的定性研究。
J Genet Couns. 2017 Dec;26(6):1324-1332. doi: 10.1007/s10897-017-0112-9. Epub 2017 May 26.
5
Committee Opinion No. 691: Carrier Screening for Genetic Conditions.第691号委员会意见:遗传性疾病的携带者筛查
Obstet Gynecol. 2017 Mar;129(3):e41-e55. doi: 10.1097/AOG.0000000000001952.
6
Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency.女性脆性X前突变:认识到原发性卵巢功能不全之外的健康挑战。
J Assist Reprod Genet. 2017 Mar;34(3):315-323. doi: 10.1007/s10815-016-0854-6. Epub 2016 Dec 19.
7
Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI).脆性X原发性卵巢功能不全(FXPOI)女性的生殖与妇科护理。
Menopause. 2016 Sep;23(9):993-9. doi: 10.1097/GME.0000000000000658.
8
Fragile X-associated tremor/ataxia syndrome - features, mechanisms and management.脆性 X 相关震颤/共济失调综合征 - 特征、机制与管理。
Nat Rev Neurol. 2016 Jul;12(7):403-12. doi: 10.1038/nrneurol.2016.82. Epub 2016 Jun 24.
9
Improving Health Education for Women Who Carry an FMR1 Premutation.改善对携带FMR1前突变女性的健康教育。
J Genet Couns. 2016 Apr;25(2):228-38. doi: 10.1007/s10897-015-9862-4. Epub 2015 Jul 16.
10
"It's got to be on this page": age and cognitive style in a study of online health information seeking.“肯定在这一页”:在线健康信息搜索研究中的年龄与认知风格
J Med Internet Res. 2015 Mar 24;17(3):e79. doi: 10.2196/jmir.3352.

携带 FMR1 前突变的男性及其健康教育需求。

Men with an FMR1 premutation and their health education needs.

机构信息

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.

Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.

出版信息

J Genet Couns. 2021 Aug;30(4):1156-1167. doi: 10.1002/jgc4.1399. Epub 2021 Mar 31.

DOI:10.1002/jgc4.1399
PMID:33788978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8363520/
Abstract

Men who carry an FMR1 premutation are at-risk to develop a late-onset neurodegenerative disorder called fragile X-Associated Ataxia/Tremor syndrome (FXTAS). However, little is known about their health informational needs. This qualitative study is the first to describe diagnostic experiences and identify specific health information needs of male premutation carriers. In-depth qualitative interviews were conducted by phone with ten men who carry an FMR1 premutation. Interviews were analyzed using direct content analysis. Saturation was assessed through use of the Comparative Method for Themes Saturation in qualitative interviews (CoMeTS). Five themes were identified: diagnosis experience, sources of health information, desired health information, barriers to obtaining health information, and facilitators to desired health information. Participants desired information about inheritance, symptoms, expectations for disease, and actions available to slow progression. Facilitators to obtaining health information included healthcare provider knowledge, positive experiences with providers, beneficial family dynamics, participating in research, and access to experts. Barriers to obtaining health information included lack of personal knowledge, lack of healthcare provider knowledge, negative experiences with providers, and uncertainty. Addressing the educational needs of men with/at-risk for FXTAS could improve the quality of life of men who carry a fragile X premutation.

摘要

携带 FMR1 前突变的男性有患上称为脆性 X 相关共济失调/震颤综合征 (FXTAS) 的迟发性神经退行性疾病的风险。然而,人们对他们的健康信息需求知之甚少。这项定性研究首次描述了男性前突变携带者的诊断经历,并确定了他们具体的健康信息需求。通过电话对十名携带 FMR1 前突变的男性进行了深入的定性访谈。使用直接内容分析法对访谈进行了分析。通过使用定性访谈的比较主题饱和度方法 (CoMeTS) 来评估饱和度。确定了五个主题:诊断经历、健康信息来源、所需健康信息、获取健康信息的障碍以及所需健康信息的促进因素。参与者希望了解遗传、症状、对疾病的预期以及可减缓疾病进展的措施。获取健康信息的促进因素包括医疗保健提供者的知识、与提供者的积极互动、有益的家庭动态、参与研究以及获得专家的帮助。获取健康信息的障碍包括个人知识的缺乏、医疗保健提供者知识的缺乏、与提供者的负面互动以及不确定性。满足患有/有风险患上 FXTAS 的男性的教育需求可以提高携带脆性 X 前突变的男性的生活质量。