Literature DB >> 18448719

Minors and informed consent in carrier testing: a survey of European clinical geneticists.

P Borry1, L Stultiens, T Goffin, H Nys, K Dierickx.   

Abstract

PURPOSE: A study was made of attitudes of clinical geneticists regarding the age at which minors should be allowed to undergo a carrier test and the reasons they provide to explain their answer.
METHODS: European clinical institutions where genetic counselling is offered to patients were contacted. 177 (63%) of the 287 eligible respondents answered a questionnaire.
RESULTS: Clinical geneticists were significantly more in favour of providing a carrier test to a younger person if the request was made together with the parents than if the adolescent requested the test personally. Although a large fraction of respondents (16%-30%) were "neither unwilling nor willing" to provide a carrier test to a 16-year-old adolescent who requested the test personally, for most disorders slightly more clinical geneticists were "very willing" or "willing".
CONCLUSION: Age is not the only decisive element when considering the participation of adolescents in decisions affecting their health. The clinical geneticists referred to cognitive, emotional and sexual maturity and the support of parents as crucial elements in their comments regarding when to tell children about their genetic risk or to allow adolescents to request a carrier test.

Entities:  

Mesh:

Year:  2008        PMID: 18448719     DOI: 10.1136/jme.2007.021717

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


  11 in total

1.  Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations.

Authors:  Pascal Borry; Gerry Evers-Kiebooms; Martina C Cornel; Angus Clarke; Kris Dierickx
Journal:  Eur J Hum Genet       Date:  2009-03-11       Impact factor: 4.246

2.  Age estimation for forensic purposes in Italy: ethical issues.

Authors:  Martina Focardi; Vilma Pinchi; Federica De Luca; Gian-Aristide Norelli
Journal:  Int J Legal Med       Date:  2014-03-16       Impact factor: 2.686

Review 3.  What is the role of genetic testing in movement disorders practice?

Authors:  Susanne A Schneider; Christine Klein
Journal:  Curr Neurol Neurosci Rep       Date:  2011-08       Impact factor: 5.081

4.  A qualitative study to explore how professionals in the United Kingdom make decisions to test children for a sickle cell carrier status.

Authors:  Melissa Noke; Sarah Peters; Alison Wearden; Fiona Ulph
Journal:  Eur J Hum Genet       Date:  2015-05-27       Impact factor: 4.246

Review 5.  Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice.

Authors:  Christopher H Wade; Beth A Tarini; Benjamin S Wilfond
Journal:  Annu Rev Genomics Hum Genet       Date:  2013-07-15       Impact factor: 8.929

6.  Developmental and behavioral pediatricians' attitudes toward screening for fragile X.

Authors:  Kruti Acharya; Abigail Schindler
Journal:  Am J Intellect Dev Disabil       Date:  2013-07

7.  Adolescent carrier testing in practice: the impact of legal rulings and problems with "gillick competence".

Authors:  Paula Boddington; Maggie Gregory
Journal:  J Genet Couns       Date:  2008-08-29       Impact factor: 2.537

8.  Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases.

Authors:  Erika Kleiderman; Bartha Maria Knoppers; Conrad V Fernandez; Kym M Boycott; Gail Ouellette; Durhane Wong-Rieger; Shelin Adam; Julie Richer; Denise Avard
Journal:  J Med Ethics       Date:  2013-12-19       Impact factor: 2.903

9.  Experiences of Women Who Have Had Carrier Testing for Duchenne Muscular Dystrophy and Becker Muscular Dystrophy During Adolescence.

Authors:  Harry G Fraser; Rebecca Z Redmond; Diana F Scotcher
Journal:  J Genet Couns       Date:  2018-07-04       Impact factor: 2.537

10.  Survey of European clinical geneticists on awareness, experiences and attitudes towards direct-to-consumer genetic testing.

Authors:  Heidi Carmen Howard; Pascal Borry
Journal:  Genome Med       Date:  2013-05-22       Impact factor: 11.117

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