Ethical dilemmas in genetic testing: examples from the Cuban program for predictive diagnosis of hereditary ataxias
- PMID: 21264501
- DOI: 10.1007/s10897-010-9347-4
Ethical dilemmas in genetic testing: examples from the Cuban program for predictive diagnosis of hereditary ataxias
Abstract
Predictive testing protocols are intended to help patients affected with hereditary conditions understand their condition and make informed reproductive choices. However, predictive protocols may expose clinicians and patients to ethical dilemmas that interfere with genetic counseling and the decision making process. This paper describes ethical dilemmas in a series of five cases involving predictive testing for hereditary ataxias in Cuba. The examples herein present evidence of the deeply controversial situations faced by both individuals at risk and professionals in charge of these predictive studies, suggesting a need for expanded guidelines to address such complexities.
Similar articles
-
Genetic testing in inherited ataxias.Semin Pediatr Neurol. 2003 Sep;10(3):223-31. doi: 10.1016/s1071-9091(03)00031-7. Semin Pediatr Neurol. 2003. PMID: 14653410 Review.
-
Ethical issues and Huntington's disease.S Afr Med J. 2013 Oct 11;103(12 Suppl 1):1023-6. doi: 10.7196/samj.7146. S Afr Med J. 2013. PMID: 24300652
-
Psychological follow-up of presymptomatic genetic testing for spinocerebellar ataxia type 2 (SCA2) in Cuba.J Genet Couns. 2007 Aug;16(4):469-79. doi: 10.1007/s10897-006-9083-y. Epub 2007 Feb 23. J Genet Couns. 2007. PMID: 17318452
-
Clinical and genetic studies of spinocerebellar ataxia type 2 in Japanese kindreds.Acta Neurol Scand. 1998 Dec;98(6):427-32. doi: 10.1111/j.1600-0404.1998.tb07325.x. Acta Neurol Scand. 1998. PMID: 9875622
-
[New insights in the molecular genetics and pathophysiology of hereditary ataxias].Nervenarzt. 1999 Jun;70(6):491-5. doi: 10.1007/s001150050470. Nervenarzt. 1999. PMID: 10412692 Review. German.
Cited by
-
Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: a systematic review.Genet Med. 2021 Dec;23(12):2270-2280. doi: 10.1038/s41436-018-0090-9. Epub 2018 Aug 3. Genet Med. 2021. PMID: 30072741
-
A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases.Prog Neurobiol. 2013 Nov;110:2-28. doi: 10.1016/j.pneurobio.2013.08.003. Epub 2013 Sep 11. Prog Neurobiol. 2013. PMID: 24036231 Free PMC article. Review.
-
Genetics Health Professionals' Views on Quality of Genetic Counseling Service Provision for Presymptomatic Testing in Late-Onset Neurological Diseases in Portugal: Core Components, Specific Challenges and the Need for Assessment Tools.J Genet Couns. 2015 Aug;24(4):616-25. doi: 10.1007/s10897-014-9784-6. Epub 2014 Nov 4. J Genet Couns. 2015. PMID: 25363284
-
What counts as effective genetic counselling for presymptomatic testing in late-onset disorders? A study of the consultand's perspective.J Genet Couns. 2013 Aug;22(4):437-47. doi: 10.1007/s10897-012-9561-3. Epub 2013 Jan 7. J Genet Couns. 2013. PMID: 23292684
-
Current Overview of Spinocerebellar Ataxia Type 7 in Mexican Population: Challenges in Specialized Care for a Rare Disease.Int J Mol Sci. 2024 Oct 6;25(19):10750. doi: 10.3390/ijms251910750. Int J Mol Sci. 2024. PMID: 39409079 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical