Literature DB >> 17943604

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

Kelly Raspberry1, Debra Skinner.   

Abstract

Because of advancements in genetic research and technologies, the clinical practice of genetics is becoming a prevalent component of biomedicine. As the genetic basis for more and more diseases are found, it is possible that ways of experiencing health, illness, identity, kin relations, and the body are becoming geneticized, or understood within a genetic model of disease. Yet, other models and relations that go beyond genetic explanations also shape interpretations of health and disease. This article explores how one group of individuals for whom genetic disorder is highly relevant formulates their views of the body in light of genetic knowledge. Using data from an ethnographic study of 106 parents or potential parents of children with known or suspected genetic disorders who were referred to a pediatric genetic counseling and evaluation clinic in the southeastern United States, we find that these parents do, to some degree, perceive of their children's disorders in terms of a genetic body that encompasses two principal qualities: a sense of predetermined health and illness and an awareness of a profound historicity that reaches into the past and extends into the present and future. They experience this genetic body as both fixed and historical, but they also express ideas of a genetic body made less deterministic by their own efforts and future possibilities. This account of parents' experiences with genetics and clinical practice contributes to a growing body of work on the ways in which genetic information and technologies are transforming popular and medical notions of the body, and with it, health, illness, kinship relations, and personal and social identities.

Entities:  

Mesh:

Year:  2007        PMID: 17943604     DOI: 10.1080/01459740701619848

Source DB:  PubMed          Journal:  Med Anthropol        ISSN: 0145-9740


  6 in total

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

Authors:  Kelly Raspberry; Debra Skinner
Journal:  Sociol Health Illn       Date:  2010-11-05

2.  The nuanced negative: Meanings of a negative diagnostic result in clinical exome sequencing.

Authors:  Debra Skinner; Kelly A Raspberry; Martha King
Journal:  Sociol Health Illn       Date:  2016-08-19

3.  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

4.  A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.

Authors:  Ian Whitmarsh; Arlene M Davis; Debra Skinner; Donald B Bailey
Journal:  Soc Sci Med       Date:  2007-06-11       Impact factor: 4.634

5.  Visualising difference, similarity and belonging in paediatric genetics.

Authors:  Janice McLaughlin; Emma K Clavering
Journal:  Sociol Health Illn       Date:  2011-11-03

6.  Systematic scoping review of the concept of 'genetic identity' and its relevance for germline modification.

Authors:  Floor M Goekoop; Carla G van El; Guy A M Widdershoven; Nadza Dzinalija; Martina C Cornel; Natalie Evans
Journal:  PLoS One       Date:  2020-01-24       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.