Preimplantation genetic testing (PGT) is a screening performed on each embryo to identify aneuploid embryos. Aneuploid embryos are embryos that do not have the correct number of chromosomes, whether it be too few or too many. An aneuploidy is the most common cause for a transferred embryo to be unsuccessful.
What does PGT test for?
PGT examines all chromosomes, including the sex chromosomes. Things we can recognize:
- Chromosomal duplications – An extra copy of chromosomes can result in conditions like down syndrome
- Chromosomal deletions – Missing copies of chromosomes
- Sex-chromosome abnormalities – Duplications or deletions of X and Y chromosomes can result in conditions like Klinefelter Syndrome and Turner Syndrome
- Gender Identification – The gender of an embryo can be identified through PGT testing
When is PGT recommended?
PGT may be recommended to you if:
- You are over 35
- You have a family history of chromosome problems
- You have a history of recurrent miscarriages
- You have had several unsuccessful cycles of IVF
The PGT process
Step 1. Normal IVF treatment is used to collect and fertilize your eggs
Step 2. The embryo is grown in the laboratory until the cells have divided and the embryo consists of enough cells to collect
Step 3. The cells are removed from the embryo for examination
Step 4. The chromosomes are examined to see how many there are and whether they are normal
Benefits of PGT
PGT testing can have numerous benefits for people looking to conceive, including:
- The number of embryos with an incorrect number of chromosomes can be minimized before implantation
- Fewer abnormal embryos transferred resulting in fewer miscarriages
- Improved implantation rates
- Reduced spontaneous abortion
For more information on PGT, call the reproductive endocrinologists at Center for Reproductive Medicine today at 612-355-8596 to schedule your first appointment.
