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1.
J Assist Reprod Genet ; 36(3): 383-393, 2019 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30554395

RESUMEN

The purpose of the paper is to explore novel means to overcome the controversial ban in the USA against mitochondrial replacement therapy, a form of IVF, with the added step of replacing a woman's diseased mutated mitochondria with a donor's healthy mitochondria to prevent debilitating and often fatal mitochondrial diseases. Long proven effective in non-human species, MRT recently performed in Mexico resulted in the birth of a healthy baby boy. We explore the ethics of the ban, the concerns over hereditability of mitochondrial disease and its mathematical basis, the overlooked role of Mitochondrial Eve, the financial burden of mitochondrial diseases for taxpayers, and a woman's reproductive rights. We examine applicable court cases, particularly protection of autonomy within the reproductive rights assured by Roe v Wade. We examine the consequences of misinterpreting MRT as genetic engineering in the congressional funding prohibitions causing the MRT ban by the FDA. Allowing MRT to take place in the USA would ensure a high standard of reproductive medicine and safety for afflicted women wishing to have genetically related children, concurrently alleviating the significant financial burden of mitochondrial diseases on its taxpayers. Since MRT does not modify any genome, it falls outside the "heritable genetic modification" terminology of concern to Congress and the FDA. Correcting this terminology, the IOM's conclusion that MRT is ethical, the continuing normalcy of the first MRT recipient, and increasing public awareness of the promising benefits might be all that is required to modify the FDA's position on MRT.


Asunto(s)
Fertilización In Vitro , Enfermedades Mitocondriales/terapia , Terapia de Reemplazo Mitocondrial , Fertilización In Vitro/ética , Fertilización In Vitro/legislación & jurisprudencia , Fertilización In Vitro/tendencias , Edición Génica/legislación & jurisprudencia , Humanos , Mitocondrias/genética , Enfermedades Mitocondriales/genética , Terapia de Reemplazo Mitocondrial/ética , Terapia de Reemplazo Mitocondrial/legislación & jurisprudencia , Terapia de Reemplazo Mitocondrial/tendencias , Estados Unidos
2.
Nat Rev Mol Cell Biol ; 19(2): 71-72, 2018 01 23.
Artículo en Inglés | MEDLINE | ID: mdl-29358685

RESUMEN

Mitochondrial DNA is maternally inherited, and pathogenic mutations cause a range of life-limiting conditions. Recent studies indicate that transmission of pathogenic mutations may be prevented by reproductive technologies designed to replace the mitochondria in eggs from affected women.


Asunto(s)
Enfermedades Mitocondriales/terapia , Terapia de Reemplazo Mitocondrial/métodos , Terapia de Reemplazo Mitocondrial/tendencias , Animales , ADN Mitocondrial/metabolismo , Femenino , Humanos , Mitocondrias/genética , Mutación/genética
4.
Trends Genet ; 32(7): 385-390, 2016 07.
Artículo en Inglés | MEDLINE | ID: mdl-27206380

RESUMEN

In 2015, the UK became the first country permitting the clinical application of mitochondrial replacement techniques (MRT). Here, we explore how MRT have led to diverging international policy. In response, we recommend focused regulatory efforts coupled with United Nations (UN) leadership to build international consensus on the future of MRT.


Asunto(s)
Epigenómica , Mitocondrias/genética , Enfermedades Mitocondriales/genética , Terapia de Reemplazo Mitocondrial/tendencias , Células Germinativas/metabolismo , Humanos , Enfermedades Mitocondriales/terapia , Reino Unido , Naciones Unidas
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