As technology advances, the relationship between society and law protecting individual autonomy and personal decisions about genetic testing becomes murky. Law regarding independent medical decisions during pregnancy and prenatal care does not always promote "autonomy"-- a multifaceted admixture of privacy rights, rights about information and the right to accept or refuse treatment. Pregnant women need information and the opportunity to exercise independent, autonomous decision-making regarding treatment during pregnancy. Yet, autonomy during pregnancy has become a rapidly moving target because new technologies affect prenatal care. Do geneticists or other technicians have any obligation to disclose risks? And if so, what are the obligations of health care professionals to ensure that the individual receiving that information understands the implications of the data transmitted? This ethical dilemma is further complicated by the unsolved question, whose information is it anyway? Is there a separate legal regime for pregnant women and children compared to other people which somehow alters their rights to information about hundreds of genetic diseases or conditions?
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Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germany
Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -As technology advances, the relationship between society and law protecting individual autonomy and personal decisions about genetic testing becomes murky. Law regarding independent medical decisions during pregnancy and prenatal care does not always promote 'autonomy'-- a multifaceted admixture of privacy rights, rights about information and the right to accept or refuse treatment. Pregnant women need information and the opportunity to exercise independent, autonomous decision-making regarding treatment during pregnancy. Yet, autonomy during pregnancy has become a rapidly moving target because new technologies affect prenatal care. Do geneticists or other technicians have any obligation to disclose risks And if so, what are the obligations of health care professionals to ensure that the individual receiving that information understands the implications of the data transmitted This ethical dilemma is further complicated by the unsolved question, whose information is it anyway Is there a separate legal regime for pregnant women and children compared to other people which somehow alters their rights to information about hundreds of genetic diseases or conditions 140 pp. Englisch. Seller Inventory # 9786200440266
Seller: moluna, Greven, Germany
Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Feitshans IliseDr. Ilise L. Feitshans, JD and ScM and DIR international health lawyer and former international civil servant at the United Nations, Geneva, Switzerland, obtained her master of science in public health from Johns Hopk. Seller Inventory # 385891712
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Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germany
Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -As technology advances, the relationship between society and law protecting individual autonomy and personal decisions about genetic testing becomes murky. Law regarding independent medical decisions during pregnancy and prenatal care does not always promote 'autonomy'-- a multifaceted admixture of privacy rights, rights about information and the right to accept or refuse treatment. Pregnant women need information and the opportunity to exercise independent, autonomous decision-making regarding treatment during pregnancy. Yet, autonomy during pregnancy has become a rapidly moving target because new technologies affect prenatal care. Do geneticists or other technicians have any obligation to disclose risks And if so, what are the obligations of health care professionals to ensure that the individual receiving that information understands the implications of the data transmitted This ethical dilemma is further complicated by the unsolved question, whose information is it anyway Is there a separate legal regime for pregnant women and children compared to other people which somehow alters their rights to information about hundreds of genetic diseases or conditions VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 140 pp. Englisch. Seller Inventory # 9786200440266
Seller: preigu, Osnabrück, Germany
Taschenbuch. Condition: Neu. Protecting Posterity: | Genetic Testing During Pregnancy and the Role of Mom's Decisionmaking | Ilise Feitshans | Taschenbuch | 140 S. | Englisch | 2019 | LAP LAMBERT Academic Publishing | EAN 9786200440266 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. Seller Inventory # 117902621
Seller: AHA-BUCH GmbH, Einbeck, Germany
Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - As technology advances, the relationship between society and law protecting individual autonomy and personal decisions about genetic testing becomes murky. Law regarding independent medical decisions during pregnancy and prenatal care does not always promote 'autonomy'-- a multifaceted admixture of privacy rights, rights about information and the right to accept or refuse treatment. Pregnant women need information and the opportunity to exercise independent, autonomous decision-making regarding treatment during pregnancy. Yet, autonomy during pregnancy has become a rapidly moving target because new technologies affect prenatal care. Do geneticists or other technicians have any obligation to disclose risks And if so, what are the obligations of health care professionals to ensure that the individual receiving that information understands the implications of the data transmitted This ethical dilemma is further complicated by the unsolved question, whose information is it anyway Is there a separate legal regime for pregnant women and children compared to other people which somehow alters their rights to information about hundreds of genetic diseases or conditions. Seller Inventory # 9786200440266
Seller: Mispah books, Redhill, SURRE, United Kingdom
paperback. Condition: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book. Seller Inventory # ERICA82962004402636