Abstract
Both researchers and clinicians are increasingly offering genomic testing for children and adolescents, a practice which parents have generally endorsed in numerous studies. By contrast, much less effort has been devoted to understanding what minors think about genetic and genomic testing. While a small number of investigators have shown that minors with or at risk for cancer generally concur with their parents and favor testing, other studies reveal that minors are less willing to participate in genomics research. Regardless, genetic and genomic testing of minors raises of host of potential legal questions. Key issues are: (1) To what extent can minors obtain genomic tests without involvement of parents or guardians? (2) To what extent can minors refuse genomic testing? and (3) To what extent can minors obtain their own results, keep their parents from getting access to them, and limit what their parents do with their genomic test results? While a number of authors have written about legal issues in genetic testing of minors, remarkably little has been written about the legal protections of minors’ choices about genomic analysis and return of results.
Publisher
Cambridge University Press (CUP)
Subject
Health Policy,General Medicine,Issues, ethics and legal aspects
Reference53 articles.
1. 22. Ark. Code Ann. § 20-9-602(7)(2013)
2. see also Ala. Code § 22-8-4, Alaska § 25.20.025(a)(2) (2013) (if parents unavailable)
3. Kan. Stat. Ann. § 38-123b(2013) (16 years old if parent not readily available)
4. La. Rev. Stat. Ann. § 40:1095 (2013) (limited to a minor "who is or believes himself to be afflicted with an illness or disease")
5. Ore. Rev. Stat. § 109.640 (2013) (15 years old)
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