Literature DB >> 21054442

Enacting genetic responsibility: experiences of mothers who carry the fragile X gene.

Kelly Raspberry1, Debra Skinner.   

Abstract

A woman who carries the gene for fragile X syndrome (FXS) has a 50 per cent chance per pregnancy of passing the gene to her sons and daughters. In this paper we analyse interview data from mothers who are carriers of the FX gene, and who have at least one child with FXS, to examine how their understandings and enactments of reproductive options, obligations, and responsibilities support an expanded notion of genetic responsibility. Accounts of 108 women from across the United States show that the majority of mothers chose not to have another biological child once they learned their carrier status. They discussed genetic responsibility and reproductive agency in terms of an obligation not to risk having another child who carried the gene, although their accounts reflected the tensions that arose from managing oneself as a genetically at-risk actor. Another 22 mothers either purposely became pregnant or continued an unplanned pregnancy after finding out their carrier status. These mothers' accounts reflect an expanded version of genetic responsibility that incorporates ideas and values beyond managing risk in what it means to act responsibly in light of genetic knowledge.
© 2010 The Authors. Sociology of Health & Illness © 2010 Foundation for the Sociology of Health & Illness/Blackwell Publishing Ltd.

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Year:  2010        PMID: 21054442      PMCID: PMC3057279          DOI: 10.1111/j.1467-9566.2010.01289.x

Source DB:  PubMed          Journal:  Sociol Health Illn        ISSN: 0141-9889


  21 in total

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3.  The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.

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4.  Guilt, blame and responsibility: men's understanding of their role in the transmission of BRCA1/2 mutations within their family.

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Journal:  Sociol Health Illn       Date:  2006-11

5.  Choosing not to choose: reproductive responses of parents of children with genetic conditions or impairments.

Authors:  Susan E Kelly
Journal:  Sociol Health Illn       Date:  2009-01

6.  Perceived quality of life in mothers of children with fragile X syndrome.

Authors:  Anne C Wheeler; Debra G Skinner; Donald B Bailey
Journal:  Am J Ment Retard       Date:  2008-05

7.  Experiencing the genetic body: parents' encounters with pediatric clinical genetics.

Authors:  Kelly Raspberry; Debra Skinner
Journal:  Med Anthropol       Date:  2007 Oct-Dec

8.  Emplotting children's lives: developmental delay vs. disability.

Authors:  Gail Landsman
Journal:  Soc Sci Med       Date:  2003-05       Impact factor: 4.634

9.  Mood and anxiety disorders in females with the FMR1 premutation.

Authors:  Jane E Roberts; Donald B Bailey; Jean Mankowski; Amy Ford; John Sideris; Leigh Anne Weisenfeld; T Morgan Heath; Robert N Golden
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2009-01-05       Impact factor: 3.568

10.  Susceptibility genes and the question of embodied identity.

Authors:  Margaret Lock; Julia Freeman; Gillian Chilibeck; Briony Beveridge; Miriam Padolsky
Journal:  Med Anthropol Q       Date:  2007-09
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  10 in total

1.  "This lifetime commitment": Public conceptions of disability and noninvasive prenatal genetic screening.

Authors:  Rosemary J Steinbach; Megan Allyse; Marsha Michie; Emily Y Liu; Mildred K Cho
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Review 2.  Does theFMR1 gene affect IVF success?

Authors:  Lisa M Pastore; Mindy S Christianson; Bailey McGuinness; Kamaria Cayton Vaught; Jacqueline Y Maher; William G Kearns
Journal:  Reprod Biomed Online       Date:  2018-12-10       Impact factor: 3.828

Review 3.  Implications of the FMR1 Premutation for Children, Adolescents, Adults, and Their Families.

Authors:  Anne Wheeler; Melissa Raspa; Randi Hagerman; Marsha Mailick; Catharine Riley
Journal:  Pediatrics       Date:  2017-06       Impact factor: 7.124

4.  The Future of Fragile X Syndrome: CDC Stakeholder Meeting Summary.

Authors:  Catharine Riley; Marsha Mailick; Elizabeth Berry-Kravis; Julie Bolen
Journal:  Pediatrics       Date:  2017-06       Impact factor: 7.124

5.  Attitudes towards potentially carrying the FMR1 premutation: before vs after testing of non-carrier females with diminished ovarian reserve.

Authors:  Lisa M Pastore; Maria Antero; Karen Ventura; J Kim Penberthy; Semara A Thomas; Logan B Karns
Journal:  J Genet Couns       Date:  2014-05-03       Impact factor: 2.537

6.  Parenting young children with and without Fragile X syndrome.

Authors:  Audra Sterling; Leah Barnum; Debra Skinner; Steven F Warren; Kandace Fleming
Journal:  Am J Intellect Dev Disabil       Date:  2012-05

7.  Public Perceptions of Ethical, Legal and Social Implications of Pre-implantation Genetic Diagnosis (PGD) in Malaysia.

Authors:  Angelina P Olesen; Siti Nurani Mohd Nor; Latifah Amin; Anisah Che Ngah
Journal:  Sci Eng Ethics       Date:  2016-12-19       Impact factor: 3.525

8.  Negotiating desires and options: how mothers who carry the fragile X gene experience reproductive decisions.

Authors:  Kelly Amanda Raspberry; Debra Skinner
Journal:  Soc Sci Med       Date:  2011-02-03       Impact factor: 4.634

9.  Preventing lives affected by hemophilia: A mixed methods study of the views of adults with hemophilia and their families toward genetic screening.

Authors:  Felicity K Boardman; Rachel Hale; Raksha Gohel; Philip J Young
Journal:  Mol Genet Genomic Med       Date:  2019-03-05       Impact factor: 2.183

10.  "I didn't take it too seriously because I'd just never heard of it": Experiential knowledge and genetic screening for thalassaemia in the UK.

Authors:  Felicity K Boardman; Rachel Hale
Journal:  J Genet Couns       Date:  2018-12-24       Impact factor: 2.537

  10 in total

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