Literature DB >> 11699548

Is there a case in favour of predictive genetic testing in young children?

S Robertson1, J Savulescu.   

Abstract

Genetic testing has brought the ability to predict the onset of diseases many years before symptoms appear and the use of such predictive testing is now widespread. The medical fraternity has met the application of this practice to children with caution. The justification for their predominantly prohibitive stance has revolved around the lack of a readily identifiable medical benefit in the face of potential psychological harms to the child. We argue that predictive testing can have important psychosocial benefits and that the interests of the child have been construed too narrowly. Proponents of a prohibitive stance also argue that testing in childhood breaches the child's future right to make the same decision as an autonomous adult and to maintain this information as confidential. We argue that predictive genetic testing of children is not necessarily a violation of the child's future autonomy. Indeed, in some cases, such testing may facilitate the development of autonomy in the maturing child. We argue that parents are generally best placed to judge what is in their own child's overall interests, and that parental request for testing after appropriate genetic counselling should be respected unless there is clear evidence that the child will be harmed in an overall sense as a result of testing.

Entities:  

Keywords:  Analytical Approach; Genetics and Reproduction

Mesh:

Year:  2001        PMID: 11699548     DOI: 10.1111/1467-8519.00210

Source DB:  PubMed          Journal:  Bioethics        ISSN: 0269-9702            Impact factor:   1.898


  35 in total

Review 1.  Research issues in genetic testing of adolescents for obesity.

Authors:  Mary E Segal; Pamela Sankar; Danielle R Reed
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Review 2.  Potential Uses and Inherent Challenges of Using Genome-Scale Sequencing to Augment Current Newborn Screening.

Authors:  Jonathan S Berg; Cynthia M Powell
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3.  Firing up the nature/nurture controversy: bioethics and genetic determinism.

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Journal:  J Med Ethics       Date:  2005-09       Impact factor: 2.903

Review 4.  Newborn screening: new developments, new dilemmas.

Authors:  N J Kerruish; S P Robertson
Journal:  J Med Ethics       Date:  2005-07       Impact factor: 2.903

Review 5.  Why tell asymptomatic children of the risk of an adult-onset disease in the family but not test them for it?

Authors:  P J Malpas
Journal:  J Med Ethics       Date:  2006-11       Impact factor: 2.903

6.  Predictive genetic testing in children: where are we now? An overview and a UK perspective.

Authors:  Anneke Lucassen; Jonathan Montgomery
Journal:  Fam Cancer       Date:  2010-03       Impact factor: 2.375

7.  Attitudes of healthcare professionals and parents regarding genetic testing for violent traits in childhood.

Authors:  E Campbell; L F Ross
Journal:  J Med Ethics       Date:  2004-12       Impact factor: 2.903

8.  Brief assessment of parents' attitudes toward testing minor children for hereditary breast/ovarian cancer genes: development and validation of the Pediatric BRCA1/2 Testing Attitudes Scale (P-TAS).

Authors:  Beth N Peshkin; Tiffani A DeMarco; Judy E Garber; Heiddis B Valdimarsdottir; Andrea F Patenaude; Katherine A Schneider; Marc D Schwartz; Kenneth P Tercyak
Journal:  J Pediatr Psychol       Date:  2008-04-01

9.  Genetic testing of children for familial cancers: a comparative legal perspective on consent, communication of information and confidentiality.

Authors:  Roy Gilbar
Journal:  Fam Cancer       Date:  2009-07-17       Impact factor: 2.375

10.  Informed decision making about predictive DNA tests: arguments for more public visibility of personal deliberations about the good life.

Authors:  Marianne Boenink; Simone van der Burg
Journal:  Med Health Care Philos       Date:  2010-05
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