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In 2011, the Istanbul Consensus Workshop on Embryo Assessment by the Alpha Scientists in Reproductive Medicine and the European Society of Human Reproduction and Embryology (ESHRE) Special Interest Group in Embryology simplified pronuclear scoring by assigning one of three classifications: symmetrical, asymmetrical and abnormal.
Pre-implantation genetic testing (PGT) can be classified as either pre-implantation genetic diagnosis (PGD) or pre-implantation genetic screening (PGS). PGS aims to improve the outcome of assisted reproductive technology (ART) treatment for the subfertile by testing for a number of the more frequent chromosome aneuploidies in an attempt to improve implantation and reduce the incidence of miscarriage. The first successful clinical application of PGD, to avoid the X-linked condition adrenoleukodystrophy, used polymerase chain reaction (PCR) to amplify a specific repeat on the Y chromosome in order to sex embryos. Patients performing embryo biopsy must be approved and licensed by the Human Fertilisation and Embryology Authority (HFEA) after inspection. The use of PGD for the prevention of transmission of serious genetic disease has largely been overtaken in volume by use of embryo biopsy to improve in vitro fertilisation (IVF) outcome for subfertile couples.
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