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
Keywords benefits  burdens  genetic counseling  health  nondirectiveness  risks  value-neutrality
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Reprint years 2004
DOI 10.1023/A:1009972728031
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Genetic Information, Rights, and Autonomy.Matti Häyry & Tuija Takala - 2001 - Theoretical Medicine and Bioethics 22 (5):403-414.

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