Genetic Testing & Carrier Screening

Preimplantation Genetic Testing
(PGT-M)

Through preimplantation genetic testing for monogenic disease or PGT-M, we can reduce the likelihood that a baby will have a known genetic disorder. It uses in vitro fertilization (IVF) to create embryos which a lab then screens for specific genetic mutations. At Fertility Specialists of Texas, our team can handle the complex and difficult cases involving PGT-M.

Stop Genetic Illness with Preimplantation Genetic Testing for Monogenic Disease, or PGT-M

About Preimplantation Genetic Testing for Monogenic Disease

When a couple has a genetic defect in their family history, they may seek PGT-M to increase the chance of having a healthy baby. After retrieving the eggs from the ovary, our laboratory fertilizes them to form embryos. Our team then performs a biopsy to remove 5-7 cells from the embryos. A lab analyzes the gene that carries the disease for the presence of the disease-causing mutation. We can then transfer those embryos that show normal biopsy results.

Limitations of PGT-M

PGT-M testing cannot screen for all genetic diseases. Additionally, it cannot determine the absence of a genetic condition with 100% certainty. During your consultation, our team will help you fully understand all aspects of treatment.

PGT-M can screen for the following conditons.