{"id":65328,"date":"2023-04-14T09:38:00","date_gmt":"2023-04-14T08:38:00","guid":{"rendered":"https:\/\/fertilityroad.com\/?p=65328"},"modified":"2023-04-27T07:39:58","modified_gmt":"2023-04-27T06:39:58","slug":"ivf-pgt-pgs-explained","status":"publish","type":"post","link":"https:\/\/fertilityroad.com\/nn\/ivf\/ivf-pgt-pgs-explained\/","title":{"rendered":"IVF with PGT-A (PGS) explained"},"content":{"rendered":"

PGT-A, which was formerly known as PGS refers to a genetic testing procedure. We consider the merits of the procedure and its use in response to your IVF questions.<\/p>\n\n\n\n

PGT-A is short for, pre-implantation genetic testing for aneuploidy. Aneuploidy refers to the existence of one or more (or missing) chromosomes which leads to unequal balance which subsequently creates health problems.<\/p>\n\n\n\n

An IVF with PGT-A \/ PGS procedure involves the biopsy of a maturing embryo to allow a genetic embryo diagnosis. The use of IVF with PGS\/PGTS-A is becoming more widespread and is offered to reassure certain patients about the genetic health of their embryo.<\/p>\n\n\n\n

IVF and preimplantation genetic tests<\/h2>\n\n\n\n

IVF with PGT-A \/ PGS is a screening method which is undertaken on an embryo after five or six days of it being created which helps the Embryologist choose the most appropriate embryo for transfer. Screening is undertaken using a variety of methods including Next Generation Sequencing (NGS), the FISH technique, or a DNA Microarray. The NGS method being the most popular as it is viewed by many to give the best results in terms of accuracy.<\/p>\n\n\n\n

During the process a number of cells are removed from each embryo (embryo biopsy) and the number of chromosomes in each embryo cell are counted. Each cell normally contains 23 pairs of chromosomes, 22 of which are the same in men and women; the 23rd chromosome, the gender chromosome dictates the sex of the embryo. The procedure will identify embryos with the correct chromosome make up as this is believed will create the best outcome for the patient and baby.<\/p>\n\n\n\n

There are many different variations of chromosomal abnormalities due to an extra or missing chromosome:<\/strong><\/p>\n\n\n\n