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.
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