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Embryo screening (PGS/PGD)

  • Preimplantation genetic screening - a screening method to improve the chance of pregnancy
  • Preimplantation genetic diagnosis - a genetic testing method to identify inherited disease
    in an embryo
IVF baby LWC Darlington

Preimplantation genetic screening (PGS)

With fewer and fewer embryos now replaced in each transfer cycle of IVF, embryo selection has become more important than ever. Traditionally, embryos are chosen according to their appearance under the microscope after three or five days of development in the incubator. However, in the past few years additional techniques of selection have been introduced which use high-tech methods to screen embryos for genetic and chromosomal information. Some studies have shown that as many as 50% of embryos are chromosomally abnormal, and, if transferred, such embryos may fail to implant in the uterus or later miscarry. The risk of chromosomal abnormalities - such as Downs syndrome - increases with maternal age.

The London Women's Clinic is able to test embryos using new techniques of embryo analysis which indicate the chromosomal status of each embryo. The idea is that only high grade embryos without chromosome abnormalities are transferred, thus reducing the risk of pregnancy failure and improving the chances of having a healthy baby.

Preimplantation genetic diagnosis (PGD)

The technique of preimplantation genetic diagnosis (PGD) can be performed successfully in couples who are known to be at risk of passing on an inherited genetic disease to their children; however, this is a complex and demanding treatment, and appropriate only for couples known to be carriers of a genetic mutation.

PGD has revolutionised the prospects of parenthood for couples who are known carriers of, for example, the cystic fibrosis gene mutation. By identifying and transferring those embryos without the mutation, carrier couples can be reassured that their baby will not be affected by a severe genetic condition.

 

 

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