Literature DB >> 10602118

Impact of genetic testing for Huntington disease on the family system.

S K Sobel1, D B Cowan.   

Abstract

The psychological impact of DNA predictive testing on asymptomatic individuals at risk for Huntington disease (HD) has received considerable attention since the advent of the procedure in 1993. This study examined the impact of such testing on families from the families' perspective. Individuals asymptomatic at the time of testing, together with their families, were interviewed in their homes with a semi-structured interview. Eighteen families with a total of 55 individuals participated. Defining the family as the unit of analysis was consistent with Systems Theory that links interactions of individuals, families, and the social environment. Areas of affected family functioning noted by the respondents included: 1) family membership; 2) family patterns of communication; and 3) future care giving concerns as they influenced current relationships. Eighty-one percent of families experienced changes in family membership. Members in 50% of families experienced changes in patterns of communication, and 56% percent of persons reported changes in current relationships in response to test results and their implications for future caregiving. The data support the conclusion that genetic testing is a family, as opposed to an individual, matter and that family involvement in the decision making process should be strongly encouraged in order to help families adjust. The data imply that families will benefit in pre-test sessions from an examination of their patterns of dealing with illness issues, both past and present. Copyright 2000 Wiley-Liss, Inc.

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Mesh:

Year:  2000        PMID: 10602118     DOI: 10.1002/(sici)1096-8628(20000103)90:1<49::aid-ajmg10>3.0.co;2-3

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  39 in total

Review 1.  Communicating genetic risk information within families: a review.

Authors:  Mel Wiseman; Caroline Dancyger; Susan Michie
Journal:  Fam Cancer       Date:  2010-12       Impact factor: 2.375

2.  A new scale to measure family members' perception of community health care services for persons with Huntington disease.

Authors:  Valmi D Sousa; Janet K Williams; Jack J Barnette; David A Reed
Journal:  J Eval Clin Pract       Date:  2010-03-11       Impact factor: 2.431

3.  (Mis)alignments in counseling for Huntington's Disease predictive testing: clients' responses to reflective frames.

Authors:  Srikant Sarangi; Kristina Bennert; Lucy Howell; Angus Clarke; Peter Harper; Jonathon Gray
Journal:  J Genet Couns       Date:  2005-02       Impact factor: 2.537

4.  Thursdays with Marion: the therapist's tale.

Authors:  Susan Sobel
Journal:  J Genet Couns       Date:  2005-10       Impact factor: 2.537

5.  What do we tell the children? Contrasting the disclosure choices of two HD families regarding risk status and predictive genetic testing.

Authors:  Kathryn Holt
Journal:  J Genet Couns       Date:  2006-08       Impact factor: 2.537

6.  More appreciation of life or regretting the test? Experiences of living as a mutation carrier of Huntington's disease.

Authors:  Anette Hagberg; The-Hung Bui; Elisabeth Winnberg
Journal:  J Genet Couns       Date:  2010-09-28       Impact factor: 2.537

7.  Family Communication in Inherited Cardiovascular Conditions in Ireland.

Authors:  Sinead Whyte; Andrew Green; Marion McAllister; Hannah Shipman
Journal:  J Genet Couns       Date:  2016-06-08       Impact factor: 2.537

8.  Role of parenting relationship quality in communicating about maternal BRCA1/2 genetic test results with children.

Authors:  Tiffani A DeMarco; Beth N Peshkin; Heiddis B Valdimarsdottir; Andrea F Patenaude; Katherine A Schneider; Kenneth P Tercyak
Journal:  J Genet Couns       Date:  2008-02-21       Impact factor: 2.537

9.  Engagement with genetic discrimination: concerns and experiences in the context of Huntington disease.

Authors:  Yvonne Bombard; Elizabeth Penziner; Oksana Suchowersky; Mark Guttman; Jane S Paulsen; Joan L Bottorff; Michael R Hayden
Journal:  Eur J Hum Genet       Date:  2007-10-24       Impact factor: 4.246

10.  Experiences of teens living in the shadow of Huntington Disease.

Authors:  Kathleen J H Sparbel; Martha Driessnack; Janet K Williams; Debra L Schutte; Toni Tripp-Reimer; Meghan McGonigal-Kenney; Lori Jarmon; Jane S Paulsen
Journal:  J Genet Couns       Date:  2008-03-18       Impact factor: 2.537

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