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Published on: June 15, 2011
Disclosing Huntington's Genetic Testing Results in the Context of Intellectual Disability and Guardianship: Using the
Mark B Warren1, Kathryn M Schak2
1Department of Psychiatry and Behavioral Sciences, Boise Veterans Administration Medical Center, University of Washington, 500 W Fort St, Boise, ID, 83702, USA. mark.warren@va.gov.
Abstract:
A diagnosis of Huntington's disease has broad social, vocational, reproductive and psychological implications. The ability to accurately diagnose the illness via genetic testing is not new. However, given a persistent lack of robustly effective interventions, it remains an area of ethical concern. The difficulty is compounded in cases of intellectual disability. This paper presents a case of genetic testing for Huntington's disease conducted on a patient with intellectual disability with guardian consent, but without the patient's direct knowledge and how the family illness narrative and psychiatric care were employed in the eventual disclosure of the patient's diagnosis and subsequent management.
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