PRESYMPTOMATIC TESTING FOR LATE-ONSET GENETIC-DISORDERS - LESSONS FROM HUNTINGTONS-DISEASE

被引:6
作者
BALL, DM
HARPER, PS
机构
[1] Institute of Medical Genetics, Univ. of Wales College of Medicine, Cardiff, Wales CF4 4XN, Heath Park
关键词
PREDICTIVE TESTING; HIGH-RISK PARENT; EARLY GENE DETECTION; LINKED MARKERS; INFORMED CONSENT;
D O I
10.1096/fasebj.6.10.1386046
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Huntington's disease is an inherited, neurodegenerative disorder, usually of adult onset. Since the identification of linked markers, more than 1000 presymptomatic tests have been performed worldwide and multiple ethical issues have been encountered in relation to informed consent, testing of children, exclusion testing during pregnancy, and confidentiality. Further ethical problems are anticipated after identification of the causal mutation (or mutations). As Huntington's disease is a model for other disorders of adult onset for which testing is becoming possible, the successful resolution of these ethical issues is of great importance. A failure to do so might discredit genetic testing as a whole.
引用
收藏
页码:2818 / 2819
页数:2
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