Genetic Health Testing and Services
Understanding your genetic health can provide peace of mind when starting a family of your own. Our experienced genetic counsellors are here to help you understand the relationship between your genetic health and fertility, as well as recommend the genetic health tests that will give you the best chance of creating a healthy family.
Genetic Health At CRGH
Our advanced reproductive genetic testing options will help you overcome known genetic conditions and ensure everything is as it should be. With our extensive genetic health expertise, we can examine your embryos during an IVF cycle to reduce the risk of miscarriage and passing down inherited genetic disorders. Non-Invasive Prenatal Testing (NIPT) will safely screen for severe congenital disorders, and CarrierMatch™ Testing can identify any genetic mutations you and your partner both carry.
No matter what type of fertility journey you’re on, genetic health testing can reduce risk and give peace of mind to single patients, same-sex couples and heterosexual couples, helping you to grow a healthy family.
Genetic Health Tests
List of services available
Genetic Counselling
Genetic counselling is often the first step for patients who want to understand more about the relationship between their genetic and reproductive health. Our experienced genetic counsellors will help you understand if there are any genetic conditions that may impact your fertility or your family, how to overcome these risks, and which tests or treatments are recommended for your fertility journey.
Learn More Here PGT-A
Preimplantation Genetic Screening for Aneuploidy (PGT-A), also known as Preimplantation Genetic Screening (PGS), involves testing embryos as part of the IVF process to screen for abnormalities. Older patients or patients who have experienced recurrent miscarriage or implantation failure often benefit from this type of genetic health testing.
Learn More About PGT-A Tests PGT-M/PGT-SR
PGT-M and PGT-SR are genetic health tests used to identify inherited genetic disorders, such as sickle cell, Huntington’s disease and cystic fibrosis. Embryos are analysed before implantation, with only healthy embryos used during fertility treatment.
Learn More Here NIPT
Non-Invasive Prenatal Testing (NIPT) uses maternal blood to screen for chromosomal abnormalities that could lead to severe congenital disorders, such as Down’s syndrome. CRGH use the most advanced NIPT available to parents, Juno’s Neo5® Test.
Learn More About NIPD Testing CarrierMatch™ Testing for Genetic Disorders
A simple blood test allows us to carry out a CarrierMatch™ test for 500 of the more common and severe genetic disorders, identifying if you and/or your partner are carriers. Our genetic counsellors will sit down with you to review your family history and provide the test results in layman’s terms.
Learn More HereBook a consultation
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