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Ethical Issues in Presymptomatic Genetic Testing for Minors: A dilemma in Li-Fraumeni Syndrome

机译:未成年人症状前基因检测的伦理问题:李-弗劳梅尼综合症的一个困境

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摘要

In 2001, a French expert panel recommended that presymptomatic tests should not be carried out on minors in families affected by Li-Fraumeni syndrome (LFS), flying in the face of possible parental demands for such testing. We decided to investigate the legitimacy of such a recommendation. We conducted a national multicenter survey using self-administered questionnaires mailed to French oncogeneticists in 33 regional centers in France. We aimed to (1) determine the extent to which these doctors were confronted with parental requests for TP53 testing, (2) study how they responded to these requests and the arguments used and (3) assess the attitude of oncogeneticists concerning the normative framework regulating the prescription of tests for minors. Twenty oncogeneticists stated that they had managed at least one LFS family. Eleven of these doctors had been confronted with parental requests for testing and three had prescribed such tests on at least one occasion. The oncogeneticists gave balanced medical, psychological and ethical arguments, highlighting the dilemma they face in the decision-making process. This dilemma is due to the lack of a consensus concerning this recommendation, which aims to protect the minor by limiting presymptomatic tests to cases in which a clear medical benefit can be demonstrated but which prevents the unique situation of particular families from being taken into account. In conclusion, the recommendation has a normative status but first, from a clinical stance, it is difficult to dissociate it from the evaluation of individual family situations, and second, the benefit of a specific medical follow-up for TP53 mutation carriers is currently being investigated.
机译:2001年,一个法国专家小组建议,在面对父母可能会要求进行此类检查的情况下,不应对受锂-弗劳梅尼综合症(LFS)影响的家庭中的未成年人进行症状前检查。我们决定调查这种建议的合法性。我们使用寄给法国33个区域中心的法国致癌基因学家的自我管理问卷进行了全国性多中心调查。我们旨在(1)确定这些医生面对父母对TP53测试的要求的程度,(2)研究他们如何回应这些要求和所使用的论点,以及(3)评估致癌基因学家对规范性框架调控的态度未成年人考试的处方。二十位致癌基因学家说,他们至少管理了一个LFS家庭。这些医生中有11名面临父母的检查要求,其中3名至少在一种情况下开了这种检查的处方。致癌基因学家给出了平衡的医学,心理和道德论据,突显了他们在决策过程中面临的困境。这种困境是由于对该建议缺乏共识,该建议旨在通过将症状明确的检查限制在可以证明有明显医疗益处的情况下,以保护未成年人,但又不能考虑到特定家庭的特殊情况。总之,该建议具有规范性地位,但首先,从临床立场来看,很难将其与评估单个家庭情况相分离,其次,目前正在对TP53突变携带者进行特定医学随访的益处调查。

著录项

  • 来源
    《Journal of Genetic Counseling》 |2013年第3期|315-322|共8页
  • 作者单位

    Laboratoire d’éthique médicale et de médecine légale Université Paris Descartes">(1);

    Département d’Oncologie de l’enfant et de l’adolescent Institut Gustave Roussy">(2);

    Laboratoire d’éthique médicale Faculté de médecine—Centre Universitaire des Saints-Pères Université Paris Descartes">(4);

    Département d’Oncologie de l’enfant et de l’adolescent Institut Gustave Roussy">(2);

    Consultation d’Oncogénétique Institut Gustave Roussy">(3);

    Consultation d’Oncogénétique Institut Gustave Roussy">(3);

    Laboratoire d’éthique médicale et de médecine légale Université Paris Descartes">(1);

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Li-Fraumeni Syndrome; Predictive genetic testing; Medical ethics; Minors;

    机译:Li-Fraumeni综合征;预测性基因检测;医学伦理学;未成年人;

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