Genetic testing in asymptomatic minors Background considerations towards ESHG Recommendations

被引:0
|
作者
Borry, Pascal [1 ]
Evers-Kiebooms, Gerry [2 ]
Cornel, Martina C. [3 ]
Clarke, Angus [4 ]
Dierickx, Kris [1 ]
机构
[1] Katholieke Univ Leuven, Fac Med, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Ctr Human Genet, Univ Hosp, Psychosocial Genet Unit, B-3000 Louvain, Belgium
[3] Vrije Univ Amsterdam, Med Ctr, EMGO Inst, Dept Clin Genet,Community Genet, Amsterdam, Netherlands
[4] Cardiff Univ, Sch Med, Inst Med Genet, Cardiff CF14 4XN, S Glam, Wales
关键词
EUROPEAN CLINICAL GENETICISTS; BEST-INTERESTS STANDARD; HEALTH-CARE SERVICES; CYSTIC-FIBROSIS; DECISION-MAKING; PARENTAL ATTITUDES; INFORMED-CONSENT; CARRIER; CHILDREN; RISK;
D O I
10.1038/ejhg.2009.25
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
Although various guidelines and position papers have discussed, in the past, the ethical aspects of genetic testing in asymptomatic minors, the European Society of Human Genetics had not earlier endorsed any set of guidelines exclusively focused on this issue. This paper has served as a background document in preparation of the development of the policy recommendations of the Public and Professional Committee of the European Society of Human Genetics. This background paper first discusses some general considerations with regard to the provision of genetic tests to minors. It discusses the concept of best interests, participation of minors in health-care decisions, parents' responsibilities to share genetic information, the role of clinical genetics and the health-care system in communication within the family. Second, it discusses, respectively, the presymptomatic and predictive genetic testing for adult-onset disorders, childhood-onset disorders and carrier testing. European Journal of Human Genetics (2009) 17, 711-719; doi: 10.1038/ejhg. 2009.25; published online 11 March 2009
引用
收藏
页码:711 / 719
页数:9
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