Doha Feto Maternal Centre

Preimplantation Genetic Screening &
Diagnosis (PGS & PGD)

Preimplantation Genetic Screening refers to the removal of one or more cells from an in vitro fertilization embryo to test for chromosomal normalcy. PGS screens the IVF embryo for a normal chromosome number

There are two kinds of PGD / PGS biopsy:

PGS allows the potential to increase I.V.F live birth success rate by screening for chromosomally normal embryos prior to transfer back to uterus.

Delay of about a month before the transfer can be done. The need for development to the Blastocyst stage is a must to do a biopsy procedure. Not all couples will have embryos develop to Blastocyst stage.

Preimplantation genetic screening refers to the removal of one or more cells from an in vitro fertilization embryo to test for chromosomal normalcy. PGS screens the embryo for a normal chromosome number. PGS is a method of chromosome disorder screening on IVF embryos.

Preimplantation genetic diagnosis involves the following steps:

There are two kinds of PGD / PGS biopsy:

We generally choose to do trophectoderm biopsy.

We generally choose to do trophectoderm biopsy.

Advantages of trophectoderm biopsy and PGD on success rates

Disadvantages of trophectoderm biopsy

disadvantages of this approach

Disadvantages of trophectoderm biopsy

disadvantages of this approach