• 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

[单基因癌症综合征的遗传咨询]

[Genetic counselling in monogenic cancer syndromes].

作者信息

Brøndum-Nielsen Karen, Gerdes Anne-Marie A

机构信息

Kennedy Instituttet--Statens Øjenklinik, Gl. Landevej 7, DK-2600 Glostrup.

出版信息

Ugeskr Laeger. 2006 Jun 12;168(24):2350-4.

PMID:16822419
Abstract

The article describes the state of the art in the management of hereditary cancer predisposition syndromes in Denmark. Genetic counselling in relation to monogenic cancer syndromes is now well established in the Danish health care system, after a remarkable development during the past 10 years. The cornerstones of this activity are identification of persons at risk through elucidation of the family history of cancer, risk assessment, genetic testing and genetic counselling of the counselee and her/his family. During the counselling process, ethical, legal and psychosocial issues are addressed. Persons identified as being at risk are offered assistance in the form of standardized screening programmes or/and prophylactic surgery, when relevant and when opted for by the patient. The ultimate purpose is to reduce cancer mortality, and the hope is that future developments will lead to the identification of effective methods of true cancer prophylaxis.

摘要

本文描述了丹麦遗传性癌症易感性综合征管理的最新状况。在过去10年取得显著发展之后,丹麦医疗保健系统中针对单基因癌症综合征的遗传咨询现已得到充分确立。这项工作的基石包括通过阐明癌症家族史来识别有风险的人群、风险评估、基因检测以及为咨询对象及其家人提供遗传咨询。在咨询过程中,会探讨伦理、法律和社会心理问题。被确定为有风险的人在相关情况下且患者选择时,会以标准化筛查计划或/和预防性手术的形式获得帮助。最终目的是降低癌症死亡率,并且希望未来的发展将带来真正有效的癌症预防方法的发现。

相似文献

1
[Genetic counselling in monogenic cancer syndromes].[单基因癌症综合征的遗传咨询]
Ugeskr Laeger. 2006 Jun 12;168(24):2350-4.
2
Organizing cancer genetics programs: the Swiss model.组织癌症遗传学项目:瑞士模式。
J Clin Oncol. 2000 Nov 1;18(21 Suppl):65S-9S.
3
[Social and family considerations in genetic counselling].[遗传咨询中的社会和家庭因素]
Ugeskr Laeger. 2006 Jun 12;168(24):2348-50.
4
Genetic counselling and genetic testing in hereditary gastrointestinal cancer syndromes.遗传性胃肠癌综合征中的遗传咨询与基因检测
Best Pract Res Clin Gastroenterol. 2009;23(2):275-83. doi: 10.1016/j.bpg.2009.02.009.
5
Adverse events in cancer genetic testing: medical, ethical, legal, and financial implications.癌症基因检测中的不良事件:医学、伦理、法律和财务影响。
Cancer J. 2012 Jul-Aug;18(4):303-9. doi: 10.1097/PPO.0b013e3182609490.
6
Establishing a cancer risk evaluation program.建立癌症风险评估项目。
Cancer Pract. 1997 Jul-Aug;5(4):228-33.
7
Experiencing genetic counselling for hereditary cancers: the client's perspective.遗传性癌症的遗传咨询体验:客户视角。
Eur J Cancer Care (Engl). 2011 Mar;20(2):204-11. doi: 10.1111/j.1365-2354.2010.01201.x.
8
[Cancer genetics: estimation of the needs of the population in France for the next ten years].[癌症遗传学:法国未来十年人口需求评估]
Bull Cancer. 2009 Sep;96(9):875-900. doi: 10.1684/bdc.2009.0943.
9
Supporting patients through genetic screening for cancer risk.通过癌症风险基因筛查为患者提供支持。
Medsurg Nurs. 2004 Aug;13(4):233-46.
10
The genetic testing process: how much counseling is needed?基因检测过程:需要多少咨询?
J Clin Oncol. 2000 Nov 1;18(21 Suppl):60S-4S.