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Prenatal Genetic Screening

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Encyclopedia of Global Bioethics
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Abstract

This entry focuses on the ethical issues of prenatal genetic screening. Genetic screening is a generic term that refers to a set of diagnostic techniques for sample collection and analysis with the aim of detecting fetal anomalies in utero. These different methods will be briefly described and assessed in terms of their ethical aspects. As one of the basic outcomes of prenatal screening is to offer parents a termination of pregnancy in case of a diseased fetus, and also because the sociocultural consequences of prenatal diagnostic technologies are highly controversial, the entry also briefly touches upon debates that relate to disability rights, eugenics, and geneticization.

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References

  • Beauchamp, T. L., & Childress, J. F. (2013). Principles of biomedical ethics. New York: Oxford University Press.

    Google Scholar 

  • Crawford, S. C. (2012). Hindu bioethics for the twenty-first century. Albany: SUNY Press.

    Google Scholar 

  • Dondorp, W., & van Lith, J. (2014). Dynamics of prenatal screening: New developments challenging the ethical framework. (editorial for a special issue in), Bioethics, 29(1), ii–iv.

    Google Scholar 

  • Duster, T. (2003). Backdoor to eugenics (2nd ed.). London: Routledge.

    Google Scholar 

  • Gigerenzer, G. (2002). Calculated risks – How to know when numbers deceive you. New York: Simon and Schuster.

    Google Scholar 

  • Green, J. M., et al. (2004). Psychosocial aspects of genetic screening of pregnant women and newborns: A systematic review. Health Technology Assessment, 8(33), 1–124.

    Google Scholar 

  • de Jong, A., et al. (2011). Advances in prenatal screening: The ethical dimension. Nature Reviews Genetics, 12, 657–663. doi:10.1038/nrg3036.

    Google Scholar 

  • Lippman, A. (1991). Prenatal genetic testing and screening: Constructing needs and reinforcing inequalities. American Journal of Law and Medicine, 17(1–2), 15–50.

    Google Scholar 

  • Nuffield Council of Bioethics. (1996). Genetic screening: The ethical issues. http://nuffieldbioethics.org/. Accessed 3 Feb 2015.

  • Paul, D. B. (1998). The politics of heredity: Essays on eugenics, biomedicine and the nature nurture debate. New York: SUNY Press.

    Google Scholar 

  • Position Statement from the Aneuploidy Screening Committee on Behalf of the Board of the International Society for Prenatal Diagnosis, April 2013. http://www.ispdhome.org/. Accessed 3 Feb 2015.

  • Sivell, S., et al. (2008). How risk is perceived, constructed and interpreted by clients in clinical genetics, and the effects on decision making: Systematic review. Journal of Genetic Counselling, 17, 30–63. doi:10.1007/s10897-007-9132-1.

    Google Scholar 

  • Geneva Foundation for Medical Education and Research. The “prenatal screening and diagnosis” entry of the online database. http://www.gfmer.ch/Guidelines/Prenatal_screening/Prenatal_screening_and_diagnosis.htm. Accessed 3 Feb 2015.

  • Wasserman, D., Bickenbach, J., & Wachbroit, R. (Eds.). (2005). Quality of life and human difference: Genetic testing, health care and disability. Cambridge: Cambridge University Press.

    Google Scholar 

Further Readings

  • Kevles, D. J. (1995). In the name of eugenics – Genetics and the uses of human heredity (2nd ed.). Cambridge, MA: Harvard University Press.

    Google Scholar 

  • Parens, E., & Asch, A. (Eds.). (2000). Prenatal testing and disability rights. Georgetown: Georgetown University Press.

    Google Scholar 

  • Robinson, P. (1998). Prenatal screening, sex selection and cloning. In H. Kuhse & P. Singer (Eds.), A companion to bioethics (pp. 173–185). London: Blackwell Publishing.

    Google Scholar 

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Correspondence to Kakuk Péter .

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© 2016 Springer International Publishing Switzerland

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Péter, K. (2016). Prenatal Genetic Screening. In: ten Have, H. (eds) Encyclopedia of Global Bioethics. Springer, Cham. https://doi.org/10.1007/978-3-319-09483-0_346

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