Negotiating Risk : : British Pakistani Experiences of Genetics / / Alison Shaw.

Drawing on fieldwork with British Pakistani clients of a UK genetics service, this book explores the personal and social implications of a ‘genetic diagnosis’. Through case material and comparative discussion, the book identifies practical ethical dilemmas raised by new genetic knowledge and shows h...

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Bibliographic Details
Superior document:Title is part of eBook package: De Gruyter Berghahn Books Complete eBook-Package 2000-2013
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Place / Publishing House:New York; , Oxford : : Berghahn Books, , [2009]
©2009
Year of Publication:2009
Language:English
Online Access:
Physical Description:1 online resource (320 p.)
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Other title:Frontmatter --
CONTENTS --
List of Figures --
Acknowledgements --
Introduction: Exploring genetic risk --
Chapter 1: Medical and public perceptions of consanguineous marriage and genetic risk --
Chapter 2: Close kin marriages: some anthropological theory and European history --
Chapter 3: British Pakistani cousin marriages: balancing marital risks --
Chapter 4: Medical surveillance and diagnostic uncertainty --
Chapter 5: Responding to reproductive risk --
Chapter 6: Foretelling and managing infant death --
Chapter 7: Genetic screening and the extended family --
Chapter 8: Genetic risk in context --
Bibliography --
Index
Summary:Drawing on fieldwork with British Pakistani clients of a UK genetics service, this book explores the personal and social implications of a ‘genetic diagnosis’. Through case material and comparative discussion, the book identifies practical ethical dilemmas raised by new genetic knowledge and shows how, while being shaped by culture, these issues also cross-cut differences of culture, religion and ethnicity. The book also demonstrates how identifying a population-level elevated ‘risk’ of genetic disorders in an ethnic minority population can reinforce existing social divisions and cultural stereotypes. The book addresses questions about the relationship between genetic risk and clinical practice that will be relevant to health workers and policy makers.
Format:Mode of access: Internet via World Wide Web.
ISBN:9781845458874
9783110998283
DOI:10.1515/9781845458874
Access:restricted access
Hierarchical level:Monograph
Statement of Responsibility: Alison Shaw.