Literature DB >> 16451127

Predictive genetic testing in young people for adult-onset conditions: where is the empirical evidence?

R E Duncan1, M B Delatycki.   

Abstract

Predictive genetic testing in young people for severe, adult-onset conditions is advised against in current guidelines. Despite this, there has been considerable debate regarding the issue. Some perceive such testing as too potentially harmful to allow. Others perceive it as an opportunity for the promotion of benefit, an opportunity even for the prevention of harm. The only way to resolve this theoretical debate is to collect empirical data related to the effects of such testing when it occurs. However, more than 15 years after the debate began, there is virtually no such empirical evidence available. The reasons for this lack of evidence appear to relate to the rarity of such testing, which when it occurs is not studied systematically. Additionally, clinicians performing such tests may feel vulnerable in sharing the outcomes, given that such testing is contrary to current recommendations. We propose a way forward that entails the provision of tests to mature minors, where clinicians deem this appropriate. These tests should be performed as part of an international research collaboration, facilitated by one leading group.

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Year:  2006        PMID: 16451127     DOI: 10.1111/j.1399-0004.2005.00505.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  18 in total

1.  The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis.

Authors:  Rony E Duncan; Lynn Gillam; Julian Savulescu; Robert Williamson; John G Rogers; Martin B Delatycki
Journal:  Fam Cancer       Date:  2009-09-17       Impact factor: 2.375

2.  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

3.  An empirical assessment of the short-term impacts of a reading of Deborah Zoe Laufer's drama Informed Consent on attitudes and intentions to participate in genetic research.

Authors:  Erin Rothwell; Jeffrey R Botkin; Sydney Cheek-O'Donnell; Bob Wong; Gretchen A Case; Erin Johnson; Trent Matheson; Alena Wilson; Nicole R Robinson; Jared Rawlings; Brooke Horejsi; Ana Maria Lopez; Carrie L Byington
Journal:  AJOB Empir Bioeth       Date:  2018-04-06

Review 4.  Ethical issues in neurogenetics.

Authors:  Wendy R Uhlmann; J Scott Roberts
Journal:  Handb Clin Neurol       Date:  2018

5.  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

6.  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

7.  Experiences of teens living in the shadow of Huntington Disease.

Authors:  Kathleen J H Sparbel; Martha Driessnack; Janet K Williams; Debra L Schutte; Toni Tripp-Reimer; Meghan McGonigal-Kenney; Lori Jarmon; Jane S Paulsen
Journal:  J Genet Couns       Date:  2008-03-18       Impact factor: 2.537

Review 8.  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

9.  Genetic counselors' perceived responsibilities regarding reproductive issues for patients at risk for Huntington disease.

Authors:  Karrie A Hines; Patricia McCarthy Veach; Bonnie S LeRoy
Journal:  J Genet Couns       Date:  2009-10-23       Impact factor: 2.537

10.  Parental attitudes and expectations towards receiving genomic test results in healthy children.

Authors:  Alanna Kulchak Rahm; Lindsay Bailey; Kara Fultz; Audrey Fan; Janet L Williams; Adam Buchanan; F Daniel Davis; Michael F Murray; Marc S Williams
Journal:  Transl Behav Med       Date:  2018-01-29       Impact factor: 3.046

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