Preimplantation genetic testing for aneuploidies (abnormal number of chromosomes) in in vitro fertilisation

S Cornelisse, M Zagers, E Kostova… - Cochrane Database …, 2020 - cochranelibrary.com
S Cornelisse, M Zagers, E Kostova, K Fleischer, M van Wely, S Mastenbroek
Cochrane Database of Systematic Reviews, 2020cochranelibrary.com
Background In in vitro fertilisation (IVF) with or without intracytoplasmic sperm injection
(ICSI), selection of the most competent embryo (s) for transfer is based on morphological
criteria. However, many women do not achieve a pregnancy even after'good quality'embryo
transfer. One of the presumed causes is that such morphologically normal embryos have an
abnormal number of chromosomes (aneuploidies). Preimplantation genetic testing for
aneuploidies (PGT‐A), formerly known as preimplantation genetic screening (PGS), was …
Background
In in vitro fertilisation (IVF) with or without intracytoplasmic sperm injection (ICSI), selection of the most competent embryo (s) for transfer is based on morphological criteria. However, many women do not achieve a pregnancy even after'good quality'embryo transfer. One of the presumed causes is that such morphologically normal embryos have an abnormal number of chromosomes (aneuploidies). Preimplantation genetic testing for aneuploidies (PGT‐A), formerly known as preimplantation genetic screening (PGS), was therefore developed as an alternative method to select embryos for transfer in IVF. In PGT‐A, the polar body or one or a few cells of the embryo are obtained by biopsy and tested. Only polar bodies and embryos that show a normal number of chromosomes are transferred.
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