Presymptomatic testing of those at 25% risk of autosomal dominant neurodegenerative disease- testing team beware
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/s41431-018-0280-6.pdf
Reference5 articles.
1. Bonnard A, Herson A, Gargiulo M, Durr A. Reverse pre-symptomatic testing for Huntington disease: double disclosure when 25% at-risk children reveal the genetic status to their parent. Eur J Hum Genet. https://doi.org/10.1038/s41431-018-0255-7 .
2. Tassicker RJ, Teltscher B, Trembath MK, Collins V, Sheffield LJ, Chiu E. et al. Problems assessing uptake of Huntington disease presymptomatic testing and a proposed solution. Eur J Hum Genet. 2009;17:66–70.
3. MacLeod R, Tibben A, Frontali M, Evers-Kiebooms G, Jones A, Martinez-Descales A. et al. Recommendations for the presymptomatic genetic test in Huntington’s disease. Clin Genet. 2013;83:221–31.
4. Almqvist EW, Bloch M, Brinkman R, Craufurd D, Hayden MR. A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after presymptomatic testing for Huntington disease. Am J Hum Genet. 1999;64:1293–304.
5. Stark Z, Wallace J, Gillam L, Burgess M, Delatycki MB. Presymptomatic genetic testing for neurodegenerative conditions: how should conflicting interests within families be managed? J Med Ethics. 2016;42:640–2.
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