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Kielstein, R. et al.

Right not to know or duty to know? Prenatal screening for polycystic renal disease.

New dimensions in different ethical scenarios following genetic information require new medical-ethical Action Guides for physician-patient interaction. This paper discusses the ambiguity in moral choice between a "right not to know" and "a duty to know", regarding parental decision-making pro or contra selective abortion following prenatal screening for autosomal dominant polycystic kidney disease (Potter III) and related public policy issues.[1]

References

Right not to know or duty to know? Prenatal screening for polycystic renal disease. Kielstein, R., Sass, H.M. The Journal of medicine and philosophy. (1992) [Pubmed]

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