Genetic Testing & IVF


During an IVF-ICSI cycle, following Egg Retrieval (OPU) and ICSI, when the egg and sperm have fertilized to form an embryo, a few cells are taken from the embryo to be tested in the Genetics Laboratory. The Embryo Transfer takes place after the results of the genetic test are released. Completing Genetic Testing during an IVF-ICSI cycle provides a wealth of information about each embryo before transferring to the uterus and does not alter the duration of treatment.

The following genetic tests may be completed during an IVF cycle:

Pre-Implantation Genetic Screening (PGS) for Chromosomal Abnormalities: Screen all 24 chromosomes for gender as well as any chromosomal abnormalities caused by missing or additional chromosomes. Chromosomal abnormalities include Trisomy 13 (Patau's syndrome), Trisomy 18 (Edward’s syndrome) and Trisomy 21 (Down syndrome). Chromosomal abnormalities are the leading cause of miscarriage.

Gender Selection: Screen your embryos to identify the gender and check for chromosomal abnormality such as Down Syndrome.

Pre-Implantation Genetic Diagnosis (PGD) for Inherited Diseases or Single Gene Disorders: Assess embryos for hereditary diseases, allowing parents with a known hereditary (genetic) disease to ensure their children do not have that genetic condition.  

HLA Matching: Curing a Family Member: Cure a family member suffering from a hereditary disease curable by bone marrow transplant by identifying an HLA Match during IVF.

If you are interested in learning more about the genetic tests available at IVF Michigan Fertility Center, email our doctors today or book an appointment to get started.