Literature DB >> 10951925

Commercial predictive testing: the desirability of one overseeing body.

R Hoedemaekers1.   

Abstract

In Europe a process of harmonisation of standards and regulations on genetic testing has started. Public discussion and consultation are recommended, but it is not clear in every European country how the decision making process as regards the further introduction of genetic testing services should be formed. In this paper the usefulness and importance of an overseeing body for genetic screening and testing is founded on four lines of reasoning: (1) analysis of the role of value judgments in the use of the concept of (genetic) abnormality; (2) a balancing of potential benefits for all parties involved; (3) a balancing of potential disadvantages, and (4) the greater availability of commercial genetic tests in the future. It is further argued that such an overseeing body has advantages for all the interested parties.

Keywords:  Euroscreen Project; Genetics and Reproduction

Mesh:

Year:  2000        PMID: 10951925      PMCID: PMC1733253          DOI: 10.1136/jme.26.4.282

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  4 in total

1.  Geneticization: the Cyprus paradigm.

Authors:  R Hoedemaekers; H ten Have
Journal:  J Med Philos       Date:  1998-06

Review 2.  The clinical introduction of genetic testing for Alzheimer disease. An ethical perspective.

Authors:  S G Post; P J Whitehouse; R H Binstock; T D Bird; S K Eckert; L A Farrer; L M Fleck; A D Gaines; E T Juengst; H Karlinsky; S Miles; T H Murray; K A Quaid; N R Relkin; A D Roses; P H St George-Hyslop; G A Sachs; B Steinbock; E F Truschke; A B Zinn
Journal:  JAMA       Date:  1997-03-12       Impact factor: 56.272

3.  National policy development for the clinical application of genetic diagnostic technologies. Lessons from cystic fibrosis.

Authors:  B S Wilfond; K Nolan
Journal:  JAMA       Date:  1993 Dec 22-29       Impact factor: 56.272

4.  The concept of abnormality in medical genetics.

Authors:  R Hoedemaekers; H ten Have
Journal:  Theor Med Bioeth       Date:  1999-12
  4 in total

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