儿科患者基因组测序的伦理思考

IF 2.4 4区医学 Q2 CLINICAL NEUROLOGY

Seminars in Pediatric Neurology Pub Date : 2023-04-01 DOI:10.1016/j.spen.2023.101039

Michelle M Sergi , Melissa C Keinath , Jonathan Fanaroff , Kathryn E Miller

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引用次数: 1

摘要

医疗环境中基因检测的进步，最近的基因组测序，增强了我们诊断遗传疾病的能力。这些进步包括基因组技术的可及性和可负担性的提高。随着使用范围的扩大，临床医生可能会面临重大的道德挑战，特别是考虑到对儿童进行一种疾病的检测和偶然发现不同疾病或健康风险的影响。在这篇重点综述中，我们讨论了从知情同意到接受基因检测儿童权利的各种伦理考虑。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Ethical Considerations of Genome Sequencing for Pediatric Patients

Advancements in genetic testing in the healthcare setting, most recently genomic sequencing, has enhanced our ability to diagnose genetic conditions. These advances include increased accessibility and affordability of genomic technologies. With expanded use comes the potential for significant ethical challenges for clinicians, particularly considering the implications of testing a child for one condition and incidentally finding a different condition or health risk. In this focused review, we address various ethical considerations from informed consent to the rights of a child undergoing genetic testing.

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来源期刊

Seminars in Pediatric Neurology CLINICAL NEUROLOGY-PEDIATRICS

CiteScore

4.80

自引率

0.00%

发文量

审稿时长

84 days

期刊介绍： Seminars in Pediatric Neurology is a topical journal that focuses on subjects of current importance in the field of pediatric neurology. The journal is devoted to making the status of such topics and the results of new investigations readily available to the practicing physician. Seminars in Pediatric Neurology is of special interest to pediatric neurologists, pediatric neuropathologists, behavioral pediatricians, and neurologists who treat all ages.