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Embryo Biopsy

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Abstract

The development of a technique for embryo biopsy that will enable the diagnosis of genetic disorders in the preimplantation embryo would represent a major advance in prenatal diagnosis (McLaren 1985; Penketh and McLaren 1987; Whittingham and Penketh 1987). Currently, such couples are faced with a number of choices: they may opt to remain childless rather than risk giving birth to an affected child; they may embark on a pregnancy, and continue with it in the hope that the fetus is unaffected; they may conceive, and opt for prenatal diagnosis (by chorionic villus sampling at 8–12 weeks’, by cordocentesis at 18–20 weeks’, or by amniocentesis at 12–18 weeks’ gestation), followed by termination of the pregnancy if the fetus is affected. This last choice may result in several cycles of conception and termination before an unaffected child is eventually conceived, or until the couple abandon all hopes of parenthood. However, if the diagnosis could be made during the preimplantation stage of embryonic development, followed by the transfer of unaffected embryos to the woman’s uterus, these distressing choices would no longer be necessary. Preimplantation diagnostic techniques, if developed, would enable couples for whom terminations are unacceptable to embark on a pregnancy in the knowledge that their future child would not be affected by the disorder for which they are at risk.

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© 1991 Springer-Verlag London Limited

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Bolton, V.N. (1991). Embryo Biopsy. In: Chapman, M.G., Grudzinskas, J.G., Chard, T. (eds) The Embryo. Springer, London. https://doi.org/10.1007/978-1-4471-1802-2_5

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  • DOI: https://doi.org/10.1007/978-1-4471-1802-2_5

  • Publisher Name: Springer, London

  • Print ISBN: 978-1-4471-1804-6

  • Online ISBN: 978-1-4471-1802-2

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