Genetic Testing
Scientific Background & Nondiscrimination Legislation
Seiten
2006
Nova Science Publishers Inc (Verlag)
978-1-59454-783-6 (ISBN)
Nova Science Publishers Inc (Verlag)
978-1-59454-783-6 (ISBN)
Collectively, genetic diseases and common diseases with a genetic component pose a significant public health burden. With completion of the human genome sequence, clinical genetic tests are becoming available at a rapid rate. This book addresses various issues surrounding genetic testing and non-discrimination.
Collectively, genetic diseases and common diseases with a genetic component pose a significant public health burden. With completion of the human genome sequence, scientists will now focus on understanding the clinical implications of the sequence information. Clinical genetic tests are becoming available at a rapid rate. Testing is regulated by the federal government and tests are beginning to be included in health insurance benefits packages. Issues surrounding genetic testing and non-discrimination addressed in this book include: What is health information and how is it currently used by health insurers and employers?; What is genetic information?; Is genetic information different from other health information?; What are the implications of having genetic information: for the individual undergoing testing? for his/her family? for society?; What evidence exists to suggest that discrimination is a problem?; Will the proposed legislation have been sufficient to protect "genetic information" and "genetic tests" that are of concern?; How does the proposed legislation compare with existing laws and regulations governing discrimination?
Collectively, genetic diseases and common diseases with a genetic component pose a significant public health burden. With completion of the human genome sequence, scientists will now focus on understanding the clinical implications of the sequence information. Clinical genetic tests are becoming available at a rapid rate. Testing is regulated by the federal government and tests are beginning to be included in health insurance benefits packages. Issues surrounding genetic testing and non-discrimination addressed in this book include: What is health information and how is it currently used by health insurers and employers?; What is genetic information?; Is genetic information different from other health information?; What are the implications of having genetic information: for the individual undergoing testing? for his/her family? for society?; What evidence exists to suggest that discrimination is a problem?; Will the proposed legislation have been sufficient to protect "genetic information" and "genetic tests" that are of concern?; How does the proposed legislation compare with existing laws and regulations governing discrimination?
Preface; Introduction; Status of Genetic Testing in the United States Public Health Significance of Genetic Conditions; Health Information; What is Genetic Information?; What Evidence Is There That Genetic Discrimination Exists?; How Do S. 306 and H.R. 1227 Compare to Existing Law?; How Would the Proposed Legislation Protect "Genetic Information"?; Title I. Health Insurance; Title II. Employment; Glossary; Index.
Erscheint lt. Verlag | 18.9.2006 |
---|---|
Zusatzinfo | Illustrations, unspecified |
Verlagsort | New York |
Sprache | englisch |
Maße | 215 x 140 mm |
Gewicht | 132 g |
Themenwelt | Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik |
Sozialwissenschaften ► Soziologie | |
ISBN-10 | 1-59454-783-1 / 1594547831 |
ISBN-13 | 978-1-59454-783-6 / 9781594547836 |
Zustand | Neuware |
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