Attitudes regarding predictive genetic testing in minors: A survey of European clinical geneticists

被引:30
作者
Borry, Pascal [1 ]
Goffin, Tom [1 ]
Nys, Herman [1 ,2 ]
Dierickx, Kris [1 ]
机构
[1] Katholieke Univ Leuven, Fac Med, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Sch Law, Louvain, Belgium
关键词
genetic testing; predictive; genetic counseling; attitudes;
D O I
10.1002/ajmg.c.30165
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The aim of this study is to gather information from European clinical geneticists about their practices and attitudes with regard to presymptomatic and predictive genetic testing in minors. European clinical institutes where genetic counseling is offered to patients were contacted. One hundred seventy-seven of the 287 eligible respondents (63%) answered a questionnaire. There was strongest support for testing young children when it provides a clear medical benefit, such as in the case of FAP and MEN2A. However, there is disagreement about when to provide predictive genetic testing for childhood-onset disorders for which therapeutic or preventive measures exist with some supporting the rule of earliest onset and others giving parents wider discretion. However, for childhood-onset disorders that do not have therapeutic measures, the majority of the respondents is unwilling to provide a presymptomatic or predictive genetic test. With respect to adolescents, many held a cautious position regarding presymptomatic and predictive genetic testing. Most clinical geneticists were unwilling to provide a presymptomatic or predictive genetic test for adult-onset diseases, except if it might provide a medical benefit. Although adolescents might be legally in the position to request a presymptomatic or predictive genetic test personally, the clinical geneticists are significantly more willing to provide a test if this request is made together with the minor's parents. This variability demonstrates the need for clinical geneticists to discuss their contradicting views and to develop harmonized practices throughout Europe. (c) 2008 Wiley-Liss, Inc.
引用
收藏
页码:78 / 83
页数:6
相关论文
共 17 条
  • [1] Huntington's disease predictive resting: The case for an assessment approach to requests from adolescents
    Binedell, J
    Soldan, JR
    Scourfield, J
    Harper, PS
    [J]. JOURNAL OF MEDICAL GENETICS, 1996, 33 (11) : 912 - 918
  • [2] Statement on genetic diagnosis in children and adolescents
    Borry, P.
    Stultiens, L.
    Nys, H.
    Cassiman, J-J
    Dierickx, K.
    [J]. CLINICAL GENETICS, 2006, 70 (05) : 374 - 381
  • [3] Guidelines for diagnosis and therapy of MEN type 1 and type 2
    Brandi, ML
    Gagel, RF
    Angeli, A
    Bilezikian, JP
    Beck-Peccoz, P
    Bordi, C
    Conte-Devolx, B
    Falchetti, A
    Gheri, RG
    Libroia, A
    Lips, CJM
    Lombardi, G
    Mannelli, M
    Pacini, F
    Pondder, BAJ
    Raue, F
    Skogseid, B
    Tamburrano, G
    Thakker, RV
    Thompson, NW
    Tomassetti, P
    Tonelli, F
    Wells, SA
    Marx, SJ
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (12) : 5658 - 5671
  • [4] Professional and personal attitudes about access and confidentiality in the genetic testing of children: A pilot study
    Campbell, E
    Ross, LF
    [J]. GENETIC TESTING, 2003, 7 (02): : 123 - 130
  • [5] THE GENETIC TESTING OF CHILDREN
    CLARKE, A
    [J]. JOURNAL OF MEDICAL GENETICS, 1994, 31 (10) : 785 - 797
  • [6] Delatycki BM, 2004, GENET TEST, V8, P98
  • [7] An international survey of predictive genetic testing in children for adult onset conditions
    Duncan, RE
    Savulescu, J
    Gillam, L
    Williamson, R
    Delatycki, MB
    [J]. GENETICS IN MEDICINE, 2005, 7 (06) : 390 - 396
  • [8] *EUR SOC HUM GEN, 2001, PROV GEN SERV EUR CU
  • [9] Presymptomatic testing in myotonic dystrophy: genetic counselling approaches
    Fokstuen, S
    Myring, J
    Evans, C
    Harper, PS
    [J]. JOURNAL OF MEDICAL GENETICS, 2001, 38 (12) : 846 - 850
  • [10] Cystic fibrosis population carrier screening: Here at last-Are we ready?
    Grody, WW
    Desnick, RJ
    [J]. GENETICS IN MEDICINE, 2001, 3 (02) : 87 - 90