Genetic Screening & Testing

At King Square Fertility, we believe informed choices lead to empowered outcomes. Our genetic screening services are designed to help individuals and couples better understand their reproductive health and potential risks - before and during fertility treatment.

Whether you’re planning for your first child or pursuing assisted reproductive options like IVF, our testing options provide vital insight into inherited conditions and embryo health.

Genetic screening helps identify whether you or your partner carries specific inherited conditions that could be passed on to your child. It can also assess embryo health during IVF to increase the chances of a successful, healthy pregnancy.

These insights support smarter decision-making, reduce uncertainty, and allow for more personalized treatment planning.

Carrier Screening

A simple blood test that identifies if you carry genes linked to conditions like cystic fibrosis, Tay-Sachs disease, or sickle cell anemia—even if you have no symptoms.

Preimplantation Genetic Testing
(PGT-A / PGT-M)

Available during IVF, PGT allows us to test embryos for chromosomal abnormalities (PGT-A) or specific inherited disorders (PGT-M) before implantation. This increases success rates and reduces the risk of miscarriage or genetic disease.

Recurrent Loss & Implantation Failure Screening

Genetic testing can help uncover chromosomal abnormalities that may contribute to repeated pregnancy loss or failed IVF cycles.

Counseling & Education

Our team provides comprehensive support, helping you understand your results and how they may impact your fertility care plan.