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Genetic discrimination and the Americans with Disabilities Act.

机译:基因歧视和《美国残疾人法》。

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摘要

Genetic discrimination is the denial of insurance, employment, or other societal benefits to an individual or members of the individual's family on the basis of real or perceived differences in that person's genetic constitution from what is considered "normal." Complex interaction between technology, law, and society has made such discrimination more and more common. Technological advances in prenatal diagnosis and genetic testing, and particularly the advent of the Human Genome Project, have resulted in a reemergence of reductionist and determinist attitudes with regard to genetic information. Such information is also perceived to be different from other medical information in that it is more personal and has greater potential for abuse. This discussion explores who is at risk of genetic discrimination and some of its potential consequences, such as the creation of a "biological underclass" of the "asymptomatic ill.".;Aspects of genetic discrimination are discussed: its sources, such as genetic testing, medical histories, and information databanks; the societal forces behind such discrimination, such as insurers, employers, and the cost of health care; and examples of these forces at work. The responses to the rise of genetic technology and genetic discrimination from groups such as professional societies, consumer advocacy groups, and legislators are also discussed. There follows a review of major federal antidiscrimination legislation including the Civil Rights Act of 1964, the Rehabilitation Act of 1973, and the Americans with Disabilities Act of 1990 (ADA).;There are several groups whose conditions are analogous to those with atypical genotypes, and which are explicitly protected by the ADA, such as cancer survivors and individuals infected with HIV. There is also evidence that the Act would protect those at risk of future illness who are currently asymptomatic. The conclusion is that, while ultimately the courts will decide, the ADA almost certainly will provide legal protection for those at risk of genetic discrimination, particularly when coupled with the emerging body of state and federal law which protects the privacy and confidentiality of genetic information.
机译:遗传歧视是基于个人的遗传构成与“正常”的真实或感知差异,剥夺个人或家庭成员的保险,就业或其他社会福利。技术,法律与社会之间复杂的相互作用使得这种歧视越来越普遍。产前诊断和基因检测的技术进步,特别是人类基因组计划的出现,导致人们对遗传信息的还原论和确定论态度重新出现。此类信息也被认为与其他医学信息不同,因为它更加个人化并具有更大的滥用可能性。讨论探讨了谁有遗传歧视的风险及其潜在的后果,例如“无症状疾病”的“生物学下层阶级”的产生。;讨论了遗传歧视的方面:其来源,如基因检测,病史和信息数据库;这种歧视背后的社会力量,例如保险公司,雇主和医疗费用;以及这些力量在起作用的例子。还讨论了诸如专业协会,消费者权益团体和立法者等团体对遗传技术兴起和遗传歧视的回应。接下来是对主要的联邦反歧视立法的审查,包括1964年的《民权法案》,1973年的《康复法案》和1990年的《美国残疾人法案》(ADA).;有些群体的病情与非典型基因型患者相似,并由ADA明确保护,例如癌症幸存者和感染HIV的个人。也有证据表明,该法案将保护那些目前没有症状,有可能患上未来疾病的人。结论是,尽管最终由法院裁决,但ADA几乎可以肯定会为有遗传歧视风险的人提供法律保护,尤其是当新兴的州和联邦法律保护了遗传信息的隐私和机密性时。

著录项

  • 作者

    Vazakas, Susan Malamate.;

  • 作者单位

    Boston University.;

  • 授予单位 Boston University.;
  • 学科 Law.;Genetics.;Philosophy.
  • 学位 Ph.D.
  • 年度 1993
  • 页码 270 p.
  • 总页数 270
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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