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.