Community Involvement in Developing Policies for Genetic Testing: Assessing the Interests and Experiences of Individuals Affected by Genetic Conditions
Paul Steven Miller
University of Washington School of Law
University of Minnesota - Twin Cities
National Institutes of Health (NIH) - National Human Genome Research Institute
January 1, 2005
Because the introduction of genetic testing into clinical medicine and public health creates concerns for the welfare of individuals affected with genetic conditions, those individuals should have a role in policy decisions about testing. Mechanisms for promoting participation range from membership on advisory committees to community dialogues to surveys that provide evidence for supporting practice guidelines. Surveys can assess the attitudes and the experiences of members of an affected group and thus inform discussions about the community’s concerns regarding the appropriate use of a genetic test. Results of a survey of individuals affected with inherited dwarfism show how data can be used in policy and clinical practice contexts. Future research into the interests of affected communities should be pursued so that underrepresented voices can be heard.
Number of Pages in PDF File: 7
Keywords: disability, community dialogue, genetic testing, public health, genetic condition, clinical researchworking papers series
Date posted: October 24, 2009
© 2014 Social Science Electronic Publishing, Inc. All Rights Reserved.
This page was processed by apollo2 in 1.610 seconds