Presymptomatic testing of those at 25% risk of autosomal dominant neurodegenerative disease- testing team beware.
作者信息
Delatycki Martin B
机构信息
Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Flemington Road, Parkville, 3052, Victoria, Australia.
出版信息
Eur J Hum Genet. 2019 Jan;27(1):20-21. doi: 10.1038/s41431-018-0280-6. Epub 2018 Oct 5.
Abstract
摘要
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本文引用的文献
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Reverse pre-symptomatic testing for Huntington disease: double disclosure when 25% at-risk children reveal the genetic status to their parent.亨廷顿病的反向症状前检测：当 25%有风险的儿童向其父母透露遗传状况时进行双重披露。
Eur J Hum Genet. 2019 Jan;27(1):22-27. doi: 10.1038/s41431-018-0255-7. Epub 2018 Sep 11.
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Predictive genetic testing for neurodegenerative conditions: how should conflicting interests within families be managed?神经退行性疾病的预测性基因检测：家庭内部的利益冲突应如何处理？
J Med Ethics. 2016 Oct;42(10):640-2. doi: 10.1136/medethics-2016-103400. Epub 2016 Jun 8.
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Recommendations for the predictive genetic test in Huntington's disease.亨廷顿舞蹈病预测性基因检测的建议。
Clin Genet. 2013 Mar;83(3):221-31. doi: 10.1111/j.1399-0004.2012.01900.x. Epub 2012 Jul 30.
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Problems assessing uptake of Huntington disease predictive testing and a proposed solution.亨廷顿病预测性检测的接受情况评估问题及一项提议的解决方案。
Eur J Hum Genet. 2009 Jan;17(1):66-70. doi: 10.1038/ejhg.2008.142. Epub 2008 Jul 30.
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A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease.对亨廷顿病预测性检测后自杀、自杀未遂或精神科住院频率的全球评估。
Am J Hum Genet. 1999 May;64(5):1293-304. doi: 10.1086/302374.
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