Abstract
The recent advances in molecular genetics have uncovered new ethical dilemmas in cancer genetics as vexed and almost certainly more complex than the disease which has up until now provoked the most debate: Huntington’s disease. Many genes that predispose to cancer have no effect until well into adult life and, as with Huntington’s, important issues arise about predictive genetic tests in fetal, childhood and adult life. Unlike Huntington’s there are sometimes options which may prevent, or at least alter the course of the disease. Nonetheless, there are hereditary cancers where little or no effective screening or treatment is possible, even when presymptomatic testing shows an individual to carry a cancer predisposing gene. Many of the lessons that have been learned from study of Huntington’s can be applied to predictive testing for cancer-predisposition genes [1].
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Evans, G., Harris, R. (1996). The ethics of testing for cancer-predisposition genes. In: Eeles, R.A., Ponder, B.A.J., Easton, D.F., Horwich, A. (eds) Genetic Predisposition to Cancer. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-4501-3_27
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DOI: https://doi.org/10.1007/978-1-4899-4501-3_27
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