Suppr超能文献

泰-萨克斯病:来自澳大利亚的当前观点

Tay-Sachs disease: current perspectives from Australia.

作者信息

Lew Raelia M, Burnett Leslie, Proos Anné L, Delatycki Martin B

机构信息

Department of Obstetrics and Gynecology, QEII Research Institute for Mothers and Infants, The University of Sydney, Australia ; Department of Obstetrics and Gynaecology, Dentistry and Health Sciences, Faculty of Medicine, The University of Melbourne, Melbourne, Australia.

NSW Health Pathology North, Royal North Shore Hospital, St Leonards, Australia ; SEALS, Prince of Wales Hospital, Randwick, Australia ; Sydney Medical School-Northern, Royal North Shore Hospital E25, University of Sydney, Sydney, Australia.

出版信息

Appl Clin Genet. 2015 Jan 21;8:19-25. doi: 10.2147/TACG.S49628. eCollection 2015.

Abstract

Tay-Sachs disease (TSD) is a fatal, recessively inherited neurodegenerative condition of infancy and early childhood. Although rare in most other populations, the carrier frequency is one in 25 in Ashkenazi Jews. Australian high-school-based TSD preconception genetic screening programs aim to screen, educate, and optimize reproductive choice for participants. These programs have demonstrated high uptake, low psychological morbidity, and have been shown to result in fewer than expected Jewish TSD-affected births over 18 years of operation. The majority of Jewish individuals of reproductive age outside of the high school screening program setting in Australia have not accessed screening. Recent recommendations advocate supplementing the community high school screening programs with general practitioner- and obstetrician-led genetic screening of Ashkenazi Jewish individuals for TSD and other severe recessive diseases for which this group is at risk. Massively parallel DNA sequencing is expected to become the testing modality of choice over the coming years.

摘要

泰-萨克斯病(TSD)是一种发生于婴幼儿期和儿童早期的致命性隐性遗传神经退行性疾病。虽然在大多数其他人群中较为罕见,但在阿什肯纳兹犹太人中,携带者频率为二十五分之一。澳大利亚以高中为基础的TSD孕前基因筛查项目旨在为参与者进行筛查、提供教育并优化生育选择。这些项目显示出参与率高、心理发病率低,并且在18年的运行中,受TSD影响的犹太裔婴儿出生数量少于预期。在澳大利亚,大多数处于生育年龄的犹太个体未参与高中筛查项目之外的筛查。最近的建议主张,通过全科医生和产科医生主导的基因筛查,对阿什肯纳兹犹太个体进行TSD及该群体面临风险的其他严重隐性疾病的筛查,以此补充社区高中筛查项目。预计在未来几年,大规模平行DNA测序将成为首选的检测方式。

相似文献

1
Tay-Sachs disease: current perspectives from Australia.泰-萨克斯病:来自澳大利亚的当前观点
Appl Clin Genet. 2015 Jan 21;8:19-25. doi: 10.2147/TACG.S49628. eCollection 2015.
9
Evaluation of a Tay-Sachs disease screening program.泰-萨克斯病筛查项目评估
Clin Genet. 2003 May;63(5):386-92. doi: 10.1034/j.1399-0004.2003.00074.x.

引用本文的文献

8
Therapeutic Strategies For Tay-Sachs Disease.泰-萨克斯病的治疗策略
Front Pharmacol. 2022 Jul 5;13:906647. doi: 10.3389/fphar.2022.906647. eCollection 2022.

本文引用的文献

3
High school Tay-Sachs disease carrier screening: 5 to 11-year follow-up.高中阶段泰-萨克斯病携带者筛查:5至11年随访
J Community Genet. 2014 Apr;5(2):139-46. doi: 10.1007/s12687-013-0163-z. Epub 2013 Jul 27.
7
Recent advances in the prenatal interrogation of the human fetal genome.人类胎儿基因组产前检测的最新进展。
Trends Genet. 2013 Feb;29(2):84-91. doi: 10.1016/j.tig.2012.10.013. Epub 2012 Nov 15.

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