Psychological Aspects of Genetic Counselling: a Review of the Experience with Huntington's Disease
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Presymptomatic DNA-testing for adult-onset diseases has serious psychological consequences. Here the psychological consequences of presymptomatic DNA-testing for Huntington's disease are reviewed. Both carriers and non-carriers experience emotional reactions after disclosure of their test result. However, up to today no long-term adverse emotional consequences have been revealed. Future research on other adult-onset genetic diseases should provide information about the reactions of children. In genetic counselling, attention should be paid to the reactions of people with a decreased risk. Genetic counselling must focus on the whole family and not on the individual applicant.
The Process of Family Reconstruction after DNA Testing for Huntington Disease.
Sobel S, Cowan D J Genet Couns. 2015; 9(3):237-51.
PMID: 26141319 DOI: 10.1023/A:1009416021896.
The right not to know: the case of psychiatric disorders.
Bortolotti L, Widdows H J Med Ethics. 2011; 37(11):673-6.
PMID: 21659442 PMC: 3197820. DOI: 10.1136/jme.2010.041111.
Stromsvik N, Nordin K, Berglund G, Engebretsen L, Hansson M, Gjengedal E J Genet Couns. 2007; 16(1):105-17.
PMID: 17277996 DOI: 10.1007/s10897-006-9047-2.
Discovering the family history of Huntington disease (HD).
Etchegary H J Genet Couns. 2006; 15(2):105-17.
PMID: 16541330 DOI: 10.1007/s10897-006-9018-7.
Population screening for hemochromatosis: has the time finally come?.
Barton J, Acton R Curr Gastroenterol Rep. 2000; 2(1):18-26.
PMID: 10980999 DOI: 10.1007/s11894-000-0047-3.