Beyond consent: ethical and social issues in genetic testing

被引:38
作者
Burgess, MM [1 ]
机构
[1] Univ British Columbia, Ctr Appl Eth, Vancouver, BC V6T 1Z2, Canada
[2] Univ British Columbia, Dept Med Genet, Vancouver, BC V6T 1Z2, Canada
关键词
D O I
10.1038/35052579
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Informed consent is a vital ethical doctrine in clinical medicine and, through genetic counselling, is being applied to genetic testing. But genetic testing raises issues that transcend the traditional concept of informed consent. Genetic tests are adopted without demonstrable clinical benefit, and the consequences of testing can reach beyond the individual to their families and communities. Understanding the social and cultural context of genetic testing will lead to more informed discussion and debate on these issues.
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收藏
页码:147 / 151
页数:5
相关论文
共 46 条
  • [1] Swiss databank to start charging for use
    Abbott, A
    [J]. NATURE, 1998, 394 (6690) : 214 - 214
  • [2] [Anonymous], GENETICS INSURANCE
  • [3] BENJAMIN CM, 1994, AM J HUM GENET, V55, P606
  • [4] The future of genetic counselling: an international perspective
    Biesecker, BB
    Marteau, TM
    [J]. NATURE GENETICS, 1999, 22 (02) : 133 - 137
  • [5] BRUNGER F, 1998, CULTURE GENETICS SOC, P30
  • [6] Burgess MM, 1996, AM J MED GENET, V62, P6, DOI 10.1002/(SICI)1096-8628(19960301)62:1<6::AID-AJMG2>3.0.CO
  • [7] 2-X
  • [8] BURGESS MM, GOVERNANCE HLTH RES
  • [9] BURGESS MM, 1999, COMMERCIALIZATION GE, P181
  • [10] BURGESS MM, 2000, GOVERNANCE HLTH RES, P14