Inherited Susceptibility to Cancer -

Inherited Susceptibility to Cancer

Clinical, Predictive and Ethical Perspectives
Buch | Softcover
472 Seiten
2009
Cambridge University Press (Verlag)
978-0-521-10474-6 (ISBN)
95,95 inkl. MwSt
Many cancers, both common and rare, are known to have a hereditary predisposition. First published in 1998, this important contribution to the literature of cancer genetics covers all the key issues, reviewing both the technology behind genetic risk assessment and the ethical dilemmas it poses.
Many cancers, both common and rare, are known to have a hereditary predisposition and advances in genetics have clarified the risks and in some cases the mechanisms of cancer developing in an individual. First published in 1998, this important contribution to the literature of cancer genetics covers all the key issues, reviewing both the technology behind genetic risk assessment and the ethical dilemmas it poses. It is divided into two parts. The first deals with ethical, legal and social issues. The second systematically outlines current knowledge of the inheritance patterns of many different cancer types, both from a site-by-site perspective and for special groups. This authoritative volume will be of interest to oncologists, physicians and surgeons in other specialities and to health professionals in the areas of primary care, counselling and cancer risk assessment.

Part I. Ethical, legal and social issues, screening, counselling, gene and mutation detection: 1. The inherited basis of cancer Shirley Hodgson and Gareth Evans; 2. Screening for cancer in those at high risk as a result of genetic susceptibility Howard Cuckle; 3. Ethical and legal perspectives on inherited cancer susceptibility Bartha Maria Knoppers and Beatrice Godard; 4. Cancer genetics and public expectations Dorothy Nelkin; 5. Genetic counselling June Peters; 6. Cancer genetics in primary care Gene Feder and Michael Modell; 7. Genetic epidemiologic approaches to finding genes that influence susceptibility to cancer Pamela St. Jean and Nicholas Schork; 8. Mutation detection Louise Hosking, Karin Au and Philippe Schork; Part II. Hereditary contribution to cancer: site-by-site and special groups: 9. Cancers of the digestive system Tamar Flanders and William Foulkes; 10. Cancers of the breast, ovary and uterus William Foulkes and Steven Narod; 11. Cancers of the kidney and urothelium Eamonn Maher; 12. Cancers of the prostate and testes Steven Narod, Bonnie King and David Hogg; 13. The neurofibromatoses and other neuro-oncological syndromes Martin Ruttledge and Guy Rouleau; 14. Malignant melanoma Nicholas Hayward; 15. Non-melanoma skin cancer David Goudie; 16. Endocrine cancers Harriet Feilotter and Lois Mulligan; 17. Tobacco-related cancers of the respiratory and upper digestive tract Zoltan Trizna and Stimson Schantz; 18. Inherited abnormalities of DNA processing and predisposition to cancer A. Malcolm Taylor; 19. Childhood cancer Kathy Pritchard-Jones; 20. Late-breaking developments William Foulkes and Shirley Hodgson; Index.

Erscheint lt. Verlag 19.3.2009
Zusatzinfo 33 Tables, unspecified; 3 Halftones, unspecified; 22 Line drawings, unspecified
Verlagsort Cambridge
Sprache englisch
Maße 152 x 229 mm
Gewicht 690 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Onkologie
Studium 2. Studienabschnitt (Klinik) Humangenetik
ISBN-10 0-521-10474-2 / 0521104742
ISBN-13 978-0-521-10474-6 / 9780521104746
Zustand Neuware
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