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A non-invasive Prenatal Test or NIPT is performed to check if your unborn child possesses certain chromosome markers that determine if your child might be at risk of Down Syndrome, Edward Syndrome, or other genetic birth abnormalities.

We recommend taking an NIPT if the either or both of the parents have been diagnosed with the above genetic abnormalities, or have a prevalence of these abnormalities in the family history.

The test is extremely accurate and completely safe for the baby as it uses the mother’s blood to find the genetic abnormalities of the unborn child.

  • Down Syndrome (trisomy 21)

  • Edward Syndrome (trysomy 18)

DNA and Genetic Profiling

We offer a full suite of DNA & genetic testing, including:

  • Whole exome sequencing

  • Targeted genetic screening and carrier status

  • Ancestry testing

  • Paternity and relationship testing

  • Lifestyle DNA profiling and precision medicine

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