Literature DB >> 17937446

The emotional effects of genetic diseases: implications for clinical genetics.

Marion McAllister1, Linda Davies, Katherine Payne, Stuart Nicholls, Dian Donnai, Rhona MacLeod.   

Abstract

The aim of this qualitative study was to explore the emotional effects that may be common to many genetic conditions, or risk of genetic conditions, that could be appropriately targeted by clinical genetics services. The study sample comprised 52 individuals. Seven focus groups with patients of clinical genetics services, their representatives from patient support organizations and genetics healthcare providers were conducted. Focus groups were supplemented by 19 face-to-face interviews with patients and patient group representatives. Focus groups and interviews were audio taped, transcribed in full, and analyzed using the constant comparative method. Eight emotional effects of genetic diseases were identified: anxiety, worry about risks to children, guilt, anger, uncertainty, sadness and grief, depression, and redemptive adjustment. Two factors were identified that could modify the emotional effects; these were variability of genetic diseases, and lack of diagnosis/inappropriate care. Despite many negative effects of genetic disease being identified, results also suggest that redemptive adjustment is possible where a genetic condition is present in a family. Interventions designed to (1) adjust the modifying conditions and (2) help manage the emotional effects may facilitate adjustment and improve patient outcomes. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17937446     DOI: 10.1002/ajmg.a.32013

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  28 in total

1.  Empowerment: qualitative underpinning of a new clinical genetics-specific patient-reported outcome.

Authors:  Marion McAllister; Graham Dunn; Chris Todd
Journal:  Eur J Hum Genet       Date:  2010-10-06       Impact factor: 4.246

2.  Stigmatization and male identity: Norwegian males' experience after identification as BRCA1/2 mutation carriers.

Authors:  Nina Strømsvik; Målfrid Råheim; Nina Oyen; Lars Fredrik Engebretsen; Eva Gjengedal
Journal:  J Genet Couns       Date:  2010-03-20       Impact factor: 2.537

3.  Impact of hereditary pancreatitis on patients and their families.

Authors:  Celeste A Shelton; Robin E Grubs; Chandraprakash Umapathy; Dhiraj Yadav; David C Whitcomb
Journal:  J Genet Couns       Date:  2020-02-05       Impact factor: 2.537

4.  Death anxiety and symbolic immortality in relatives at risk for familial amyloid polyneuropathy type I (FAP I, ATTR V30M).

Authors:  Paula I Santos; Eurico Figueiredo; Inês Gomes; Jorge Sequeiros
Journal:  J Genet Couns       Date:  2010-08-03       Impact factor: 2.537

5.  Concerns about inherited risk of breast cancer prior to diagnosis in Japanese patients with breast complaints.

Authors:  Noriko Ando; Yumi Iwamitsu; Masaru Kuranami; Shigemi Okazaki; Kenji Yamamoto; Masahiko Watanabe; Hitoshi Miyaoka
Journal:  Fam Cancer       Date:  2011-12       Impact factor: 2.375

6.  The Subjective Experience of Patients Diagnosed with Hereditary Hemorrhagic Telangiectasia: a Qualitative Study.

Authors:  Laura Geerts; Carole Fantini-Hauwel; Elodie Brugallé; Odile Boute; Frédéric Frénois; Lydie Defrance; Sylvie Manouvrier-Hanu; Florence Petit; Pascal Antoine
Journal:  J Genet Couns       Date:  2016-10-28       Impact factor: 2.537

7.  Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.

Authors:  Allyn McConkie Rosell; Loren D M Pena; Kelly Schoch; Rebecca Spillmann; Jennifer Sullivan; Stephen R Hooper; Yong-Hui Jiang; Nicolas Mathey-Andrews; David B Goldstein; Vandana Shashi
Journal:  J Genet Couns       Date:  2016-02-12       Impact factor: 2.537

8.  An exploration of the experience of Huntington's disease in family dyads: an interpretative phenomenological analysis.

Authors:  Caroline Maxted; Jane Simpson; Stephen Weatherhead
Journal:  J Genet Couns       Date:  2013-11-10       Impact factor: 2.537

9.  Perceptions of the concept of mutation among family members of patients receiving outpatient genetic services and university students.

Authors:  Noriko Ando; Yumi Iwamitsu; Kazuhisa Takemura; Yukiko Saito; Fumio Takada
Journal:  J Genet Couns       Date:  2009-09-25       Impact factor: 2.537

10.  "My Plate is Full": Reasons for Declining a Genetic Evaluation of Hearing Loss.

Authors:  Marci M Lesperance; Erin Winkler; Tori L Melendez; Beverly M Yashar
Journal:  J Genet Couns       Date:  2017-10-04       Impact factor: 2.537

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