Negotiating Risk - Alison Shaw

Negotiating Risk

British Pakistani Experiences of Genetics

(Autor)

Buch | Hardcover
320 Seiten
2009
Berghahn Books (Verlag)
978-1-84545-548-4 (ISBN)
139,50 inkl. MwSt
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...
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.

Alison Shaw is Senior Research Fellow at the Ethox Centre, University of Oxford, having taught at Brunel (1997-2004), London and Oxford Brookes universities. Her research interests include medical anthropology, ethnicity, kinship and social aspects of genetics. Her books include Kinship and Continuity: Pakistani families in Britain (Routledge 2000); A Pakistani Community in Britain (Blackwell 1888); and Changing Sex and Bending Gender (Berghahn 2005), edited with Shirley Ardener.

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

Erscheint lt. Verlag 1.1.2009
Verlagsort Oxford
Sprache englisch
Maße 152 x 229 mm
Gewicht 562 g
Themenwelt Studium 2. Studienabschnitt (Klinik) Humangenetik
Sozialwissenschaften Ethnologie
Sozialwissenschaften Soziologie
ISBN-10 1-84545-548-7 / 1845455487
ISBN-13 978-1-84545-548-4 / 9781845455484
Zustand Neuware
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