Literature DB >> 26141319

The Process of Family Reconstruction after DNA Testing for Huntington Disease.

S Sobel1, D B Cowan.   

Abstract

The needs of families to reconstruct their relationships in response to the DNA testing for Huntington disease of one or more of their asymptomatic members are presented. Data were collected from family interviews with 18 families, and from their responses on a post interview questionnaire. Findings are that families need to (a) address "unfinished business" associated with the decision for testing; (b) bring family members, peripheral in the decision for testing, into the loop; (c) reorganize patterns of communication and roles altered by the testing and heal ruptures in family membership; and (d) revise family stories about illness to provide a meaning for HD and explain the test results in a way that leaves them with a sense of mastery. Findings suggest that families should be more involved in the initial decision for testing of a member and that protocols should be established to provide help for their ongoing adjustment.

Entities:  

Year:  2000        PMID: 26141319     DOI: 10.1023/A:1009416021896

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  24 in total

1.  Genetic testing of families with hereditary diseases.

Authors:  A Wexler
Journal:  JAMA       Date:  1996-10-09       Impact factor: 56.272

2.  Reactions to predictive testing in Huntington disease: case reports of coping with a new genetic status.

Authors:  T B Wahlin; A Lundin; L Bäckman; E Almqvist; A Haegermark; B Winblad; M Anvret
Journal:  Am J Med Genet       Date:  1997-12-19

3.  Family process, chronic illness, and death. On the weakness of strong bonds.

Authors:  D Reiss; S Gonzalez; N Kramer
Journal:  Arch Gen Psychiatry       Date:  1986-08

Review 4.  Predictive testing for Huntington disease: a psychologist's view.

Authors:  S Kessler
Journal:  Am J Med Genet       Date:  1994-09-15

Review 5.  Psychological aspects of genetic counselling: a review of the experience with Huntington's disease.

Authors:  A van 't Spijker; H F ten Kroode
Journal:  Patient Educ Couns       Date:  1997 Sep-Oct

6.  Chronic illness and the life cycle: a conceptual framework.

Authors:  J S Rolland
Journal:  Fam Process       Date:  1987-06

7.  Predictive testing for Huntington disease in Canada: adverse effects and unexpected results in those receiving a decreased risk.

Authors:  M Huggins; M Bloch; S Wiggins; S Adam; O Suchowersky; M Trew; M Klimek; C R Greenberg; M Eleff; L P Thompson
Journal:  Am J Med Genet       Date:  1992-02-15

8.  Psychiatric implications of presymptomatic testing for Huntington's disease.

Authors:  Seymour Kessler
Journal:  Am J Orthopsychiatry       Date:  1987-04

9.  Patient, family, and staff responses to end-stage renal disease.

Authors:  D Reiss
Journal:  Am J Kidney Dis       Date:  1990-03       Impact factor: 8.860

10.  Presymptomatic testing for huntington diseases: Recommendations for counseling.

Authors:  K A Quaid
Journal:  J Genet Couns       Date:  1992-12       Impact factor: 2.537

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  3 in total

1.  Families' experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population.

Authors:  Álvaro Mendes; Liliana Sousa
Journal:  Fam Cancer       Date:  2012-06       Impact factor: 2.375

2.  Family matters: examining a multi-family group intervention for women with BRCA mutations in the scope of genetic counselling.

Authors:  Alvaro Mendes; Raquel Chiquelho; Teresa Almeida Santos; Liliana Sousa
Journal:  J Community Genet       Date:  2010-10-05

3.  Role of older generations in the family's adjustment to Huntington disease.

Authors:  Carla Roma Oliveira; Álvaro Mendes; Jorge Sequeiros; Liliana Sousa
Journal:  J Community Genet       Date:  2021-03-25
  3 in total

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