Literature DB >> 17712355

Attitudes regarding carrier testing in incompetent children: a survey of European clinical geneticists.

Pascal Borry1, Tom Goffin, Herman Nys, Kris Dierickx.   

Abstract

The aim of this study is to gather information from European clinical geneticists about their practices and attitudes with regard to carrier testing in incompetent children. European clinical institutes where genetic counseling is offered to patients have been contacted. One hundred and seventy-seven of the 287 eligible respondents, corresponding to a response rate of 63%, completed the questionnaire. For all autosomal recessive and X-linked disorders studied, the majority of the respondents were very unwilling or unwilling to provide a carrier test to a 6-year-old asymptomatic child on parental request (range 73-91%). The results of the Wilcoxon-Mann-Whitney U test indicated that for almost all disorders, respondents from Eastern and Southern European countries are more willing to provide a carrier test to a 6-year-old asymptomatic child than respondents from Western and Northern European countries. The Spearman's rank correlation coefficients showed that when a clinical geneticist was unwilling to perform such a test, he/she mostly disagreed that parental uncertainty and anxiety was a good reason to perform a carrier test, he/she mostly disagreed that parents should have the right to decide about such a test, he/she mostly agreed that future autonomy and the confidentiality of genetic information is violated if this test is performed. Overall, the survey showed an adherence to existing recommendations and guidelines regarding carrier testing in incompetent minors. However, for every condition studied, a group of clinical geneticists was willing or very willing to provide a carrier test to a 6-year-old child on parental request.

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Year:  2007        PMID: 17712355     DOI: 10.1038/sj.ejhg.5201909

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  14 in total

1.  A qualitative study exploring genetic counsellors' experiences of counselling children.

Authors:  Fiona Ulph; James Leong; Cris Glazebrook; Ellen Townsend
Journal:  Eur J Hum Genet       Date:  2010-06-09       Impact factor: 4.246

2.  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

3.  Quality in genetic counselling for presymptomatic testing--clinical guidelines for practice across the range of genetic conditions.

Authors:  Heather Skirton; Lesley Goldsmith; Leigh Jackson; Aad Tibben
Journal:  Eur J Hum Genet       Date:  2012-08-15       Impact factor: 4.246

4.  "They Just Want to Know" - Genetic Health Professionals' Beliefs About Why Parents Want to Know their Child's Carrier Status.

Authors:  Danya F Vears; Clare Delany; John Massie; Lynn Gillam
Journal:  J Genet Couns       Date:  2017-02-04       Impact factor: 2.537

5.  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

6.  Why Do Parents Want to Know their Child's Carrier Status? A Qualitative Study.

Authors:  Danya F Vears; Clare Delany; John Massie; Lynn Gillam
Journal:  J Genet Couns       Date:  2016-05-19       Impact factor: 2.537

7.  When to tell and test for genetic carrier status: perspectives of adolescents and young adults from fragile X families.

Authors:  Ramsey M Wehbe; Gail A Spiridigliozzi; Elizabeth M Heise; Deborah V Dawson; Allyn McConkie-Rosell
Journal:  Am J Med Genet A       Date:  2009-06       Impact factor: 2.802

8.  Professional ambivalence: accounts of ethical practice in childhood genetic testing.

Authors:  Michael Arribas-Ayllon; Srikant Sarangi; Angus Clarke
Journal:  J Genet Couns       Date:  2009-02-10       Impact factor: 2.537

9.  Disparities in current and future childhood and newborn carrier identification.

Authors:  Melissa Noke; Alison Wearden; Sarah Peters; Fiona Ulph
Journal:  J Genet Couns       Date:  2014-07-11       Impact factor: 2.537

10.  Carrier testing in children: exploration of genetic health professionals' practices in Australia.

Authors:  Danya F Vears; Clare Delany; Lynn Gillam
Journal:  Genet Med       Date:  2014-09-18       Impact factor: 8.822

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