Suppr超能文献

短讯:关于一种罕见眼病基因检测的亲身经历观点

Short Communication: Lived experience perspectives on genetic testing for a rare eye disease.

作者信息

Tam Mallorie T, Daboub Alonso, Lou Hayami, Robillard Julie M

机构信息

Department of Medicine, Division of Neurology, University of British Columbia, Vancouver, BC, Canada.

BC Children's and Women's Hospital, Vancouver, BC, Canada.

出版信息

J Community Genet. 2024 Feb;15(1):97-101. doi: 10.1007/s12687-023-00677-5. Epub 2023 Oct 3.

Abstract

This qualitative study explored the motivators and barriers for genetic testing for individuals with aniridia. Semi-structured interviews were conducted with 8 participants. The main findings highlighted the complex and interrelated factors involved in the decision-making process, including family planning, learning about the specific pathogenic variant of the disease and having access to genetic testing. Benefits and potential risks of genetic testing for aniridia were also discussed. For participants, gaining knowledge about their condition was perceived as a benefit, while administrative issues and concerns around privacy were identified as risks. Increased access to quality information about genetic testing and to the service and associated resources are needed to better support people living with aniridia.

摘要

这项定性研究探讨了无虹膜症患者进行基因检测的动机和障碍。对8名参与者进行了半结构化访谈。主要研究结果突出了决策过程中涉及的复杂且相互关联的因素,包括计划生育、了解疾病的特定致病变体以及获得基因检测。还讨论了无虹膜症基因检测的益处和潜在风险。对参与者而言,了解自身病情被视为一种益处,而行政问题和对隐私的担忧则被确定为风险。需要增加获取有关基因检测的高质量信息以及服务和相关资源的机会,以更好地支持无虹膜症患者。

相似文献

1
Short Communication: Lived experience perspectives on genetic testing for a rare eye disease.
J Community Genet. 2024 Feb;15(1):97-101. doi: 10.1007/s12687-023-00677-5. Epub 2023 Oct 3.
2
Parent decision-making around the genetic testing of children for germline TP53 mutations.
Cancer. 2015 Jan 15;121(2):286-93. doi: 10.1002/cncr.29027. Epub 2014 Sep 15.
7
Exploring the Experiences of Autistic Transgender and Non-Binary Adults in Seeking Gender Identity Health Care.
Autism Adulthood. 2023 Jun 1;5(2):191-203. doi: 10.1089/aut.2023.0003. Epub 2023 Jun 13.
8
Public perception of predictive cancer genetic testing and research in Oregon.
J Genet Couns. 2020 Apr;29(2):259-281. doi: 10.1002/jgc4.1262. Epub 2020 Mar 27.
10
CMS-01 Genetic testing for familial amyotrophic lateral sclerosis (ALS): insights and challenges.
Amyotroph Lateral Scler Frontotemporal Degener. 2019 Nov;20(sup1):327-347. doi: 10.1080/21678421.2019.1647002.

引用本文的文献

1
Psychosocial Factors Involved in Genetic Testing for Rare Diseases: A Scoping Review.
Genes (Basel). 2025 May 22;16(6):614. doi: 10.3390/genes16060614.

本文引用的文献

1
"I am not a number!" Opinions and preferences of people with intellectual disability about genetic healthcare.
Eur J Hum Genet. 2023 Sep;31(9):1057-1065. doi: 10.1038/s41431-023-01282-3. Epub 2023 Jan 20.
2
Congenital aniridia beyond black eyes: From phenotype and novel genetic mechanisms to innovative therapeutic approaches.
Prog Retin Eye Res. 2023 Jul;95:101133. doi: 10.1016/j.preteyeres.2022.101133. Epub 2022 Oct 22.
3
Survey of perspectives of people with inherited retinal diseases on ocular gene therapy in Australia.
Gene Ther. 2023 Apr;30(3-4):336-346. doi: 10.1038/s41434-022-00364-z. Epub 2022 Oct 2.
5
Access to genetic testing for rare diseases: Existing gaps in public-facing information.
World Med Health Policy. 2021 Sep;13(3):518-525. doi: 10.1002/wmh3.469. Epub 2021 Jul 26.
7
Clinical utility gene card for: Aniridia.
Eur J Hum Genet. 2016 Nov;24(11). doi: 10.1038/ejhg.2016.73. Epub 2016 Jul 6.
8
Progress and prospects of next-generation sequencing testing for inherited retinal dystrophy.
Expert Rev Mol Diagn. 2015;15(10):1269-75. doi: 10.1586/14737159.2015.1081057. Epub 2015 Aug 26.
9
Communicating the promise for ocular gene therapies: challenges and recommendations.
Am J Ophthalmol. 2015 Sep;160(3):408-415.e2. doi: 10.1016/j.ajo.2015.05.026. Epub 2015 May 30.
10
Genetic testing for inherited eye disease: who benefits?
JAMA Ophthalmol. 2013 Oct;131(10):1265-6. doi: 10.1001/jamaophthalmol.2013.4509.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验