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Anticipated stigma and blameless guilt: Mothers' evaluation of life with the sex-linked disorder, hypohidrotic ectodermal dysplasia (XHED)

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  • Clarke, Angus

Abstract

Practical experience of a genetic disorder may influence how parents approach reproduction, if they know their child may be affected by an inherited condition. One important aspect of this practical experience is the stigmatisation which family members may experience or witness. We outline the concept of stigma and how it affects those in families with a condition that impacts upon physical appearance. We then consider the accounts given by females in families affected by the rare sex-linked disorder, X-linked hypohidrotic ectodermal dysplasia (XHED), which principally affects males but can be passed through female carriers to affect their sons. The stigmatisation of affected males is as important in the accounts given by their womenfolk as the physical effects of the condition; this impacts on their talk about transmission of the disorder to the next generation.

Suggested Citation

  • Clarke, Angus, 2016. "Anticipated stigma and blameless guilt: Mothers' evaluation of life with the sex-linked disorder, hypohidrotic ectodermal dysplasia (XHED)," Social Science & Medicine, Elsevier, vol. 158(C), pages 141-148.
  • Handle: RePEc:eee:socmed:v:158:y:2016:i:c:p:141-148
    DOI: 10.1016/j.socscimed.2016.04.027
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    References listed on IDEAS

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    1. Pescosolido, Bernice A. & Martin, Jack K. & Lang, Annie & Olafsdottir, Sigrun, 2008. "Rethinking theoretical approaches to stigma: A Framework Integrating Normative Influences on Stigma (FINIS)," Social Science & Medicine, Elsevier, vol. 67(3), pages 431-440, August.
    2. Boardman, Felicity Kate, 2014. "The expressivist objection to prenatal testing: The experiences of families living with genetic disease," Social Science & Medicine, Elsevier, vol. 107(C), pages 18-25.
    3. Shostak, Sara & Zarhin, Dana & Ottman, Ruth, 2011. "What's at stake? Genetic information from the perspective of people with epilepsy and their family members," Social Science & Medicine, Elsevier, vol. 73(5), pages 645-654, September.
    4. Kenen, R.H. & Schmidt, R.M., 1978. "Stigmatization of carrier status: Social implications of heterozygote genetic screening programs," American Journal of Public Health, American Public Health Association, vol. 68(11), pages 1116-1120.
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    1. Mendes, Álvaro & Sousa, Liliana & Sequeiros, Jorge & Clarke, Angus, 2017. "Discredited legacy: Stigma and familial amyloid polyneuropathy in Northwestern Portugal," Social Science & Medicine, Elsevier, vol. 182(C), pages 73-80.

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