Medicine, Health Care and Philosophy 4 (1):47-51 (2001)
Abstract |
Beginning with a discussion of why value neutrality on the part of the genetics counselor does not necessarily preserve autonomy of the counselee, the idea that social values unavoidably underlie the articulation of risks and benefits of genetic testing is made explicit. Despite the best efforts of a counselor to convey value neutral facts, risk assessment by the counselee and family is done according to normative analysis, experience with illness, and definitions of health. Each of these factors must be known by the genetic counselor in order to relate those facts which she acknowledges as relevant to the decisions that will be made by those people seeking the genetic information
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Keywords | benefits burdens genetic counseling health nondirectiveness risks value-neutrality |
Categories | (categorize this paper) |
Reprint years | 2004 |
DOI | 10.1023/A:1009972728031 |
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Microethics: The Ethics of Everyday Clinical Practice.Robert D. Truog, Stephen D. Brown, David Browning, Edward M. Hundert, Elizabeth A. Rider, Sigall K. Bell & Elaine C. Meyer - 2015 - Hastings Center Report 45 (1):11-17.
Genetic Information, Rights, and Autonomy.Matti Häyry & Tuija Takala - 2001 - Theoretical Medicine and Bioethics 22 (5):403-414.
Informed Consent and the Misattributed Paternity Problem in Genetic Counseling.Erica K. Lucast - 2007 - Bioethics 21 (1):41–50.
Bioethical Concepts in Theory and Practice: An Exploratory Study of Prenatal Screening in Iceland. [REVIEW]Helga Gottfreðsdóttir & Vilhjálmur Árnason - 2011 - Medicine, Health Care and Philosophy 14 (1):53-61.
Geneticization and Bioethics: Advancing Debate and Research. [REVIEW]Vilhjálmur Árnason & Stefán Hjörleifsson - 2007 - Medicine, Health Care and Philosophy 10 (4):417-431.
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