• 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

乳腺癌和卵巢癌的遗传易感性:一项病例研究。

Genetic predisposition to breast and ovarian cancer: a case study.

作者信息

Amlung S, Huelsman K, Skinn B

机构信息

Institute for Nursing Research, College of Nursing, University of Cincinnati, West Chester, OH 45069, USA.

出版信息

AACN Clin Issues. 1998 Nov;9(4):555-62. doi: 10.1097/00044067-199811000-00010.

DOI:10.1097/00044067-199811000-00010
PMID:9855865
Abstract

Information concerning genetic predisposition and the discovery of genes associated with certain cancer risks is changing rapidly. Nurses must keep abreast of these changes so that they can better understand the choices patients have and the consequences of those choices. This article discusses the issues pertinent to women with a genetic predisposition to breast or ovarian cancer, or both. Discoveries in the Human Genome Project have already begun to change traditional perspectives on screening, diagnosing, preventing, and treating cancer. These genetic discoveries hold both promise and concern for health care professionals. The promise lies in the precise identification of genetic predisposition to common diseases and the potential to prevent or reduce morbidity and mortality rates. The concern lies in issues of confidentiality and discrimination: Predicting predisposition to incurable illnesses may have substantial negative impact on the person's quality of life and psychosocial integrity.

摘要

有关遗传易感性以及与某些癌症风险相关基因的发现正在迅速变化。护士必须跟上这些变化,以便能更好地理解患者所面临的选择以及这些选择的后果。本文讨论了与有乳腺癌或卵巢癌或两者遗传易感性的女性相关的问题。人类基因组计划中的发现已经开始改变对癌症筛查、诊断、预防和治疗的传统观念。这些基因发现给医疗保健专业人员带来了希望和担忧。希望在于能够精确识别常见疾病的遗传易感性,以及预防或降低发病率和死亡率的潜力。担忧在于保密和歧视问题:预测对不治之症的易感性可能会对个人的生活质量和心理社会完整性产生重大负面影响。

相似文献

1
Genetic predisposition to breast and ovarian cancer: a case study.乳腺癌和卵巢癌的遗传易感性:一项病例研究。
AACN Clin Issues. 1998 Nov;9(4):555-62. doi: 10.1097/00044067-199811000-00010.
2
Informed consent for BRCA1 and BRCA2 testing: what clinicians should know about the process and content.
J Am Med Womens Assoc (1972). 2000 Fall;55(5):275-9.
3
Factors associated with decisions about clinical BRCA1/2 testing.与临床BRCA1/2检测决策相关的因素。
Cancer Epidemiol Biomarkers Prev. 2000 Nov;9(11):1251-4.
4
Genetic testing for breast cancer predisposition.乳腺癌易感性的基因检测
Surg Clin North Am. 1999 Oct;79(5):1171-87, xxi. doi: 10.1016/s0039-6109(05)70067-0.
5
BRCA1 and BRCA2 testing: weighing the demand against the benefits.BRCA1和BRCA2检测:权衡需求与益处。
Am J Hum Genet. 1999 Apr;64(4):943-8. doi: 10.1086/302350.
6
Germline mutations in BRCA1 and BRCA2 in breast-ovarian families from a breast cancer risk evaluation clinic.来自一家乳腺癌风险评估诊所的乳腺-卵巢癌家族中BRCA1和BRCA2的种系突变。
J Clin Oncol. 2001 Apr 15;19(8):2247-53. doi: 10.1200/JCO.2001.19.8.2247.
7
Deleterious mutations of both BRCA1 and BRCA2 in three siblings.三名兄弟姐妹中BRCA1和BRCA2的有害突变。
Genet Test. 1998;2(1):75-7. doi: 10.1089/gte.1998.2.75.
8
Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study.一项基于人群的研究中除BRCA1和BRCA2外的其他乳腺癌易感基因的证据。
Genet Epidemiol. 2001 Jul;21(1):1-18. doi: 10.1002/gepi.1014.
9
BRCA1/BRCA2 mutations and breast cancer in Ashkenazi Jewish women.阿什肯纳兹犹太女性中的BRCA1/BRCA2基因突变与乳腺癌
Ann N Y Acad Sci. 1997 Dec 29;833:198-203. doi: 10.1111/j.1749-6632.1997.tb48610.x.
10
Breast & ovarian cancer. Issues in risk assessment.乳腺癌与卵巢癌。风险评估问题。
Adv Nurse Pract. 1999 Aug;7(8):26-32; quiz 33-4.