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Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences.
Quarrell, Oliver W; Clarke, Angus J; Compton, Cecilia; de Die-Smulders, Christine E M; Fryer, Alan; Jenkins, Sian; Lahiri, Nayana; MacLeod, Rhona; Miedzybrodzka, Zosia; Morrison, Patrick J; Musgrave, Hannah; O'Driscoll, Mary; Strong, Mark; van Belzen, Martine J; Vermeer, Sascha; Verschuuren-Bemelmans, Corien C; Bijlsma, Emilia K.
  • Quarrell OW; Department of Clinical Genetics, Sheffield Children's Hospital, Northern General Hospital, Sheffield, UK.
  • Clarke AJ; Division of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UK.
  • Compton C; University of London and St George's University Hospitals NHS Foundation Trust, Institute of Molecular and Clinical Sciences, London, UK.
  • de Die-Smulders CEM; Department of Clinical Genetics, Maastricht Universitair Medisch Centrum, Maastricht, The Netherlands.
  • Fryer A; Liverpool Women's Hospital NHS Foundation Trust, Liverpool, UK.
  • Jenkins S; Department Clinical Genetics, University Hospital of Southampton, Oxford Eye Hospital, Oxford, UK.
  • Lahiri N; University of London and St. George's Hospital, Institute of Molecular and Clinical Sciences, London, UK.
  • MacLeod R; Manchester Centre for Genomic Medicine, St Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Center, Manchester, UK.
  • Miedzybrodzka Z; School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK.
  • Morrison PJ; Centre for Cancer Research and Cell Biology, Queens University Belfast, Belfast, UK.
  • Musgrave H; Department of Clinical Genetics, Yorkshire Regional Genetics Service, Chapel Allerton Hospital, Leeds, UK.
  • O'Driscoll M; West midlands Regional Clinical genetics service and Birmingham Health Partners Birmingham Women's Hospital NHS Foundation Trust, Birmingham, UK.
  • Strong M; School of Health and Related Research, University of Sheffield, Sheffield, UK.
  • van Belzen MJ; Department of Clinical Genetics, Leids Universitair Medisch Centrum, Leiden, The Netherlands.
  • Vermeer S; Radboud University Medical Center, Nijmegen, The Netherlands.
  • Verschuuren-Bemelmans CC; Department of Genetics, Universitair Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • Bijlsma EK; Department of Clinical Genetics, Leids Universitair Medisch Centrum, Leiden, The Netherlands.
Am J Med Genet B Neuropsychiatr Genet ; 177(1): 35-39, 2018 Jan.
Article en En | MEDLINE | ID: mdl-29095566
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedad de Huntington Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Female / Humans / Male País como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedad de Huntington Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Female / Humans / Male País como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article