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Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences.

Quarrell, OW; Clarke, AJ; Compton, C; de Die-Smulders, CEM; Fryer, A; Jenkins, S; Lahiri, N; MacLeod, R; Miedzybrodzka, Z; Morrison, PJ; et al. Quarrell, OW; Clarke, AJ; Compton, C; de Die-Smulders, CEM; Fryer, A; Jenkins, S; Lahiri, N; MacLeod, R; Miedzybrodzka, Z; Morrison, PJ; Musgrave, H; O'Driscoll, M; Strong, M; van Belzen, MJ; Vermeer, S; Verschuuren-Bemelmans, CC; Bijlsma, EK (2017) Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences. Am J Med Genet B Neuropsychiatr Genet, 177 (1). pp. 35-39. ISSN 1552-485X https://doi.org/10.1002/ajmg.b.32582
SGUL Authors: Lahiri, Nayana

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Abstract

A consistent feature of predictive testing guidelines for Huntington's disease (HD) is the recommendation not to undertake predictive tests on those < 18 years. Exceptions are made but the extent of, and reasons for, deviation from the guidelines are unknown. The UK Huntington's Prediction Consortium has collected data annually on predictive tests undertaken from the 23 UK genetic centers. DNA analysis for HD in the Netherlands is centralized in the Laboratory for Diagnostic Genome Analysis in Leiden. In the UK, 60 tests were performed on minors between 1994 and 2015 representing 0.63% of the total number of tests performed. In the Netherlands, 23 tests were performed on minors between 1997 and 2016. The majority of the tests were performed on those aged 16 and 17 years for both countries (23% and 57% for the UK, and 26% and 57% for the Netherlands). Data on the reasons for testing were identified for 36 UK and 22 Netherlands cases and included: close to the age of 18 years, pregnancy, currently in local authority care and likely to have less support available after 18 years, person never having the capacity to consent and other miscellaneous reasons. This study documents the extent of HD testing of minors in the UK and the Netherlands and suggests that, in general, the recommendation is being followed. We provide some empirical evidence as to reasons why clinicians have departed from the recommendation. We do not advise changing the recommendation but suggest that testing of minors continues to be monitored.

Item Type: Article
Additional Information: This is the peer reviewed version of the following article: Quarrell, OW, Clarke, AJ, Compton, C, et al. Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences. Am J Med Genet Part B. 2018; 177B: 35– 39, which has been published in final form at https://doi.org/10.1002/ajmg.b.32582. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Keywords: CAG, children, genetic tests, teenagers, Adolescent, Female, Genetic Testing, Humans, Huntington Disease, Male, Minors, Netherlands, United Kingdom, Humans, Huntington Disease, Adolescent, Minors, Netherlands, Female, Male, Genetic Testing, United Kingdom, CAG, children, genetic tests, teenagers, CAG, children, genetic tests, teenagers, 0604 Genetics, 1103 Clinical Sciences, 1109 Neurosciences
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical & Biomedical Education (IMBE)
Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Clinical Education (INMECE )
Journal or Publication Title: Am J Med Genet B Neuropsychiatr Genet
ISSN: 1552-485X
Language: eng
Dates:
DateEvent
12 December 2017Published
2 November 2017Published Online
10 July 2017Accepted
Publisher License: Publisher's own licence
PubMed ID: 29095566
Web of Science ID: WOS:000417876700004
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/110977
Publisher's version: https://doi.org/10.1002/ajmg.b.32582

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