Reproductive Genetic Testing

Empowering Your Journey to Parenthood with Clarity and Confidence.

Building a family is one of life’s most profound journeys, but it often comes with questions. Reproductive genetic testing provides the answers you need to move forward with confidence. By analyzing the genetic health of embryos or prospective parents, we help illuminate the path toward a healthy pregnancy.

Whether you are exploring carrier screening before conception or Preimplantation Genetic Testing (PGT) during IVF, our mission is simple: to replace uncertainty with insight. We combine compassionate care with advanced science to give your future family the best possible start.

Preimplantation Genetic Testing

Preimplantation Genetic Testing (PGT) is a sophisticated screening procedure performed on embryos during an In Vitro Fertilization (IVF) cycle. By analyzing a small sample of cells from a developing embryo (typically at the blastocyst stage), clinicians can identify genetic abnormalities before a pregnancy is established.

The primary goal of PGT is to provide more information about the genetic health of an embryo, helping patients and physicians select the most viable embryo for transfer, thereby increasing the likelihood of a successful pregnancy and the birth of a healthy baby.

 

Carrier Screening

Carrier screening is a genetic test used to determine if an individual carries a gene mutation for a specific inherited disorder. While carriers typically do not show any symptoms and are often unaware of their genetic status, they can pass the mutation on to their children.

This screening is most commonly performed before or during pregnancy to help prospective parents understand the risk of having a child with a genetic condition.

 

Whole Genome Sequencing

By providing a complete genetic blueprint, WGS serves as a foundational tool for proactive and personalized healthcare. It shifts the medical focus from reactive treatment to predictive prevention.