Preimplantation Genetic Screening: A Practical Guide
Author(s) -
Paul R. Brezina,
Raymond W. Ke,
William H. Kutteh
Publication year - 2013
Publication title -
clinical medicine insights reproductive health
Language(s) - English
Resource type - Journals
ISSN - 1179-5581
DOI - 10.4137/cmrh.s10852
Subject(s) - sophistication , genetic testing , in vitro fertilisation , aneuploidy , preimplantation genetic diagnosis , biology , reproductive medicine , embryo , medicine , genetics , pregnancy , sociology , social science , chromosome , gene
The past several decades have seen tremendous advances in the field of medical genetics. The application of genetic technologies to the field of reproductive medicine has ushered in a new era of medicine that is likely to greatly expand in the coming years. Concurrent with an in vitro fertilization (IVF) cycle, it is now possible to obtain a cellular biopsy from a developing embryo and genetically evaluate this sample with increasing sophistication and detail. Preimplantation genetic screening (PGS) is the practice of determining the presence of aneuploidy (either too many or too few chromosomes) in a developing embryo. However, how and in whom PGS should be offered is a topic of much debate.
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