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成人发病疾病的产前检测:美国国家遗传咨询师协会的立场

Prenatal Testing for Adult-Onset Conditions: the Position of the National Society of Genetic Counselors.

作者信息

Hercher Laura, Uhlmann Wendy R, Hoffman Erin P, Gustafson Shanna, Chen Kelly M

机构信息

Joan H. Marks Graduate Program in Human Genetics, Sarah Lawrence College, NY, USA.

Department of Internal Medicine and Department of Human Genetics, University of Michigan, Ann Arbor, MI, 48109, USA.

出版信息

J Genet Couns. 2016 Dec;25(6):1139-1145. doi: 10.1007/s10897-016-9992-3. Epub 2016 Jul 1.

Abstract

Advances in genetic testing and the availability of such testing in pregnancy allows prospective parents to test their future child for adult-onset conditions. This ability raises several complex ethical issues. Prospective parents have reproductive rights to obtain information about their fetus. This information may or may not alter pregnancy management. These rights can be in conflict with the rights of the future individual, who will be denied the right to elect or decline testing. This paper highlights the complexity of these issues, details discussions that went into the National Society of Genetic Counselors (NSGC) Public Policy Task Force's development of the Prenatal testing for Adult-Onset Conditions position statement adopted in November 2014, and cites relevant literature on this topic through December 2015. Issues addressed include parental rights and autonomy, rights of the future child, the right not to know, possible adverse effects on childhood and the need for genetic counseling. This paper will serve as a reference to genetic counselors and healthcare professionals when faced with this situation in clinical practice.

摘要

基因检测技术的进步以及孕期可进行此类检测,使得准父母能够为其未来的孩子检测成年后才会出现的疾病。这种能力引发了若干复杂的伦理问题。准父母拥有获取有关其胎儿信息的生育权利。这些信息可能会也可能不会改变孕期管理方式。这些权利可能会与未来个体的权利相冲突,因为未来个体将被剥夺选择接受或拒绝检测的权利。本文强调了这些问题的复杂性,详细阐述了美国国家遗传咨询师协会(NSGC)公共政策特别工作组在制定2014年11月通过的《成人发病疾病的产前检测》立场声明时所进行的讨论,并引用了截至2015年12月关于该主题的相关文献。所涉及的问题包括父母的权利与自主权、未来孩子的权利、不知情权、对儿童可能产生的不利影响以及遗传咨询的必要性。本文将为遗传咨询师和医疗保健专业人员在临床实践中遇到这种情况时提供参考。

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