Literature DB >> 16850280

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

Kathryn Holt1.   

Abstract

Above all else, predictive genetic testing provides information. Gaining insight into the psychosocial effects of this information is a primary goal of genetic counseling. For individuals utilizing predictive genetic testing, the acquisition of genetic information requires choices regarding disclosure within the family. This study uses a phenomenological methodology to explore the contrasting choices of two sets of HD parents regarding the disclosure of genetic risk status to their children. Additionally, the children (now adults) discuss their lived experience growing up with contrasting disclosure dynamics, and their current views regarding the use of predictive genetic testing for themselves. The primary finding of this study is that all of the adult children now express preference for early disclosure of genetic risk and an open/supportive communication style regarding HD. This finding has value for clinicians working with HD families who must make decisions regarding disclosure issues related to predictive genetic testing.

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Year:  2006        PMID: 16850280     DOI: 10.1007/s10897-006-9021-z

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


  22 in total

1.  Psychiatric management of Huntington's disease in extended care settings.

Authors:  Brian E Wood; Kye K Kim; Gary J Harpold
Journal:  Psychiatr Serv       Date:  2002-06       Impact factor: 3.084

2.  Effects of communication skills training on parents and young adolescents from extreme family types.

Authors:  Susan K Riesch; Jeffrey Henriques; Weena Chanchong
Journal:  J Child Adolesc Psychiatr Nurs       Date:  2003 Oct-Dec

Review 3.  Elements of a genetics counseling service.

Authors:  Noelle Agan; Anthony R Gregg
Journal:  Obstet Gynecol Clin North Am       Date:  2002-06       Impact factor: 2.844

4.  Living with Huntington's disease: need for supportive care.

Authors:  Sky Dawson; Linda J Kristjanson; Christine M Toye; Penny Flett
Journal:  Nurs Health Sci       Date:  2004-06       Impact factor: 1.857

Review 5.  Psychological consequences of predictive genetic testing: a systematic review.

Authors:  M Broadstock; S Michie; T Marteau
Journal:  Eur J Hum Genet       Date:  2000-10       Impact factor: 4.246

6.  Predictive DNA-testing for Huntington's disease and reproductive decision making: a European collaborative study.

Authors:  Gerry Evers-Kiebooms; Kurt Nys; Peter Harper; Moniek Zoeteweij; Alexandra Dürr; Gioia Jacopini; Christos Yapijakis; Sheila Simpson
Journal:  Eur J Hum Genet       Date:  2002-03       Impact factor: 4.246

7.  A hereditary disorder in the family and the family life cycle: Huntington disease as a paradigm.

Authors:  A Christine Brouwer-Dudokdewit; Anke Savenije; Moniek W Zoeteweij; Anneke Maat-Kievit; Aad Tibben
Journal:  Fam Process       Date:  2002

8.  Molecular analysis and clinical correlations of the Huntington's disease mutation.

Authors:  J C MacMillan; R G Snell; A Tyler; G D Houlihan; I Fenton; J P Cheadle; L P Lazarou; D J Shaw; P S Harper
Journal:  Lancet       Date:  1993-10-16       Impact factor: 79.321

9.  Effects of individual and family functioning on interest in genetic testing.

Authors:  Deborah J Bowen; Emily Bourcier; Nancy Press; Frances M Lewis; Wylie Burke
Journal:  Community Genet       Date:  2004

10.  We are talking, but are they listening? Communication patterns in families with a history of breast/ovarian cancer (HBOC).

Authors:  Regina Kenen; Audrey Arden-Jones; Rosalind Eeles
Journal:  Psychooncology       Date:  2004-05       Impact factor: 3.894

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  15 in total

1.  Communication of genetic risk information to daughters in families with fragile X syndrome: the parent's perspective.

Authors:  Allyn McConkie-Rosell; Jacqueline Del Giorno; Elizabeth Melvin Heise
Journal:  J Genet Couns       Date:  2010-09-28       Impact factor: 2.537

2.  Decision-making about inherited cancer risk: exploring dimensions of genetic responsibility.

Authors:  Holly Etchegary; Fiona Miller; Sonya deLaat; Brenda Wilson; June Carroll; Mario Cappelli
Journal:  J Genet Couns       Date:  2009-03-18       Impact factor: 2.537

3.  Amyotrophic lateral sclerosis in a patient with a family history of huntington disease: genetic counseling challenges.

Authors:  Andrea L Smith; James W Teener; Brian C Callaghan; Jack Harrington; Wendy R Uhlmann
Journal:  J Genet Couns       Date:  2014-04-26       Impact factor: 2.537

Review 4.  What facilitates or impedes family communication following genetic testing for cancer risk? A systematic review and meta-synthesis of primary qualitative research.

Authors:  Kim Chivers Seymour; Julia Addington-Hall; Anneke M Lucassen; Claire L Foster
Journal:  J Genet Couns       Date:  2010-04-09       Impact factor: 2.537

5.  Ethics in prion disease.

Authors:  Kendra Bechtel; Michael D Geschwind
Journal:  Prog Neurobiol       Date:  2013-07-29       Impact factor: 11.685

6.  Communication about Congenital Adrenal Hyperplasia: Perspective of Filipino Families.

Authors:  Peter James B Abad; Cora A Anonuevo; Sandra Daack-Hirsch; Lorna R Abad; Carmencita D Padilla; Mercy Y Laurino
Journal:  J Genet Couns       Date:  2016-11-10       Impact factor: 2.537

7.  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

8.  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

9.  Genetic risk communication: experiences of adolescent girls and young women from families with fragile X syndrome.

Authors:  Allyn McConkie-Rosell; Elizabeth Melvin Heise; Gail A Spiridigliozzi
Journal:  J Genet Couns       Date:  2009-03-11       Impact factor: 2.537

10.  A family genetic risk communication framework: guiding tool development in genetics health services.

Authors:  Miriam E Wiens; Brenda J Wilson; Christina Honeywell; Holly Etchegary
Journal:  J Community Genet       Date:  2013-01-15
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