Literature DB >> 19277061

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

Pascal Borry1, Gerry Evers-Kiebooms, Martina C Cornel, Angus Clarke, Kris Dierickx.   

Abstract

Although various guidelines and position papers have discussed, in the past, the ethical aspects of genetic testing in asymptomatic minors, the European Society of Human Genetics had not earlier endorsed any set of guidelines exclusively focused on this issue. This paper has served as a background document in preparation of the development of the policy recommendations of the Public and Professional Committee of the European Society of Human Genetics. This background paper first discusses some general considerations with regard to the provision of genetic tests to minors. It discusses the concept of best interests, participation of minors in health-care decisions, parents' responsibilities to share genetic information, the role of clinical genetics and the health-care system in communication within the family. Second, it discusses, respectively, the presymptomatic and predictive genetic testing for adult-onset disorders, childhood-onset disorders and carrier testing.

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Year:  2009        PMID: 19277061      PMCID: PMC2947094          DOI: 10.1038/ejhg.2009.25

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


  71 in total

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Journal:  Med Health Care Philos       Date:  2002

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3.  Deliberate deceit of family members: a challenge to providers of clinical genetics services.

Authors:  Jennifer T Loud; Nancy E Weissman; June A Peters; Ruthann M Giusti; Benjamin S Wilfond; Wylie Burke; Mark H Greene
Journal:  J Clin Oncol       Date:  2006-04-01       Impact factor: 44.544

4.  The genetic testing of children. Working Party of the Clinical Genetics Society (UK)

Authors:  A Clarke
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

5.  GIG response to the UK Clinical Genetics Society report "The genetic testing of children".

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Journal:  J Med Genet       Date:  1995-06       Impact factor: 6.318

6.  The impact of population based screening for carriers of cystic fibrosis.

Authors:  H Bekker; G Denniss; M Modell; M Bobrow; T Marteau
Journal:  J Med Genet       Date:  1994-05       Impact factor: 6.318

7.  Newborn screening: complexities in universal genetic testing.

Authors:  Nancy S Green; Siobhan M Dolan; Thomas H Murray
Journal:  Am J Public Health       Date:  2006-03-29       Impact factor: 9.308

8.  Attitudes toward the genetic testing of children among adults in a Utah-based kindred tested for a BRCA1 mutation.

Authors:  H A Hamann; R T Croyle; V L Venne; B J Baty; K R Smith; J R Botkin
Journal:  Am J Med Genet       Date:  2000-05-01

9.  The use of preventive health care services: carrier testing for the genetic disorder haemophilia.

Authors:  I Varekamp; T P Suurmeijer; F R Rosendaal; A H Bröcker-Vriends
Journal:  Soc Sci Med       Date:  1993-09       Impact factor: 4.634

10.  Informed consent, parental permission, and assent in pediatric practice. Committee on Bioethics, American Academy of Pediatrics.

Authors: 
Journal:  Pediatrics       Date:  1995-02       Impact factor: 7.124

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  56 in total

1.  Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.

Authors:  Maartje C Van Rij; Marjan De Rademaeker; Céline Moutou; Jos C F M Dreesen; Martine De Rycke; Inge Liebaers; Joep P M Geraedts; Christine E M De Die-Smulders; Stéphane Viville
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

2.  Challenges of genetic testing in adolescents with cardiac arrhythmia syndromes.

Authors:  Lilian Liou Cohen; Marina Stolerman; Christine Walsh; David Wasserman; Siobhan M Dolan
Journal:  J Med Ethics       Date:  2011-09-27       Impact factor: 2.903

3.  Psychosocial Adjustment in School-age Girls With a Family History of Breast Cancer.

Authors:  Angela R Bradbury; Linda Patrick-Miller; Lisa Schwartz; Brian Egleston; Colleen Burke Sands; Wendy K Chung; Gord Glendon; Jasmine A McDonald; Cynthia Moore; Paula Rauch; Lisa Tuchman; Irene L Andrulis; Saundra S Buys; Caren J Frost; Theresa H M Keegan; Julia A Knight; Mary Beth Terry; Esther M John; Mary B Daly
Journal:  Pediatrics       Date:  2015-10-19       Impact factor: 7.124

4.  Attitudes to reproductive genetic testing in women who had a positive BRCA test before having children: a qualitative analysis.

Authors:  Elizabeth Ormondroyd; Louise Donnelly; Clare Moynihan; Cornelie Savona; Elizabeth Bancroft; D Gareth Evans; Rosalind Eeles; Stuart Lavery; Maggie Watson
Journal:  Eur J Hum Genet       Date:  2011-08-03       Impact factor: 4.246

Review 5.  Impact of presymptomatic genetic testing on young adults: a systematic review.

Authors:  Lea Godino; Daniela Turchetti; Leigh Jackson; Catherine Hennessy; Heather Skirton
Journal:  Eur J Hum Genet       Date:  2015-07-15       Impact factor: 4.246

6.  Newborn Sequencing in Genomic Medicine and Public Health.

Authors:  Jonathan S Berg; Pankaj B Agrawal; Donald B Bailey; Alan H Beggs; Steven E Brenner; Amy M Brower; Julie A Cakici; Ozge Ceyhan-Birsoy; Kee Chan; Flavia Chen; Robert J Currier; Dmitry Dukhovny; Robert C Green; Julie Harris-Wai; Ingrid A Holm; Brenda Iglesias; Galen Joseph; Stephen F Kingsmore; Barbara A Koenig; Pui-Yan Kwok; John Lantos; Steven J Leeder; Megan A Lewis; Amy L McGuire; Laura V Milko; Sean D Mooney; Richard B Parad; Stacey Pereira; Joshua Petrikin; Bradford C Powell; Cynthia M Powell; Jennifer M Puck; Heidi L Rehm; Neil Risch; Myra Roche; Joseph T Shieh; Narayanan Veeraraghavan; Michael S Watson; Laurel Willig; Timothy W Yu; Tiina Urv; Anastasia L Wise
Journal:  Pediatrics       Date:  2017-01-17       Impact factor: 7.124

7.  Presymptomatic genetic testing for hereditary cancer in young adults: a survey of young adults and parents.

Authors:  Lea Godino; Daniela Turchetti; Leigh Jackson; Catherine Hennessy; Heather Skirton
Journal:  Eur J Hum Genet       Date:  2018-10-04       Impact factor: 4.246

8.  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

9.  Carrier detection in childhood: a need for policy reform.

Authors:  Lainie Friedman Ross
Journal:  Genome Med       Date:  2010-04-22       Impact factor: 11.117

10.  Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their child.

Authors:  Candice Cornelis; Aad Tibben; Wybo Dondorp; Mieke van Haelst; Annelien L Bredenoord; Nine Knoers; Marcus Düwell; Ineke Bolt; Marieke van Summeren
Journal:  Eur J Hum Genet       Date:  2016-07-27       Impact factor: 4.246

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