「遺伝情報」の家族-集団間共有性と遺伝病告知の対象拡大 : 誰が「遺伝情報」に対する権利を有するのか?
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概要
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Through focusing on issues such as the expansion of warning targets of their genetic diseases and the enforcement of involuntary genetic testing, this article brings forth the discussion that the sharable nature of "genetic infor mation" among families and the community does not only leverage the genetic privacy of individuals, but also has the possibility to diminish such privacy. As mentioned in this article, in Safer v. The Estate of George T. Pack, 677 A.2d 1188 (N.J. 1996), the court imposed a duty to a doctor professing in genetic diseases to warn the patient and the families of the patient of genetic risks. Moreover, in consideration to the polysemic nature of "genetic information," this article debates the restriction of sharing such information in case of involuntary genetic testing, and refers to the possibility of comprehensive argument on the "genetic privacy" issue, only through specific classification or typification of "genetic information" itself.
- 日本法政学会の論文
- 2005-05-15
日本法政学会 | 論文
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