Understanding Female Infertility — Free Webinar · 22 Oct · 6:30 PM (AEDT)
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  • Genetic Testing

    Genetic testing is important because abnormal chromosomes can stop an embryo from implanting on the uterine lining, or result in a miscarriage or the birth of a child with physical and/or mental disabilities. Testing can help prevent these outcomes by identifying the affected embryos during their development in the laboratory, before they are transferred back to a patient’s uterus during an IVF cycle.

    At City Fertility we pride ourselves on offering the latest techniques to give our patients the best care and maximise their chances of falling pregnant.
    This approach includes genetic testing of IVF embryos, and this page is designed to give you a valuable insight into the process, along with its benefits, risks and alternatives.
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    Genetic Testing Methods

    There are two methods of genetic testing:

    • Preimplantation Genetic Testing for Aneuploidy (PGT-A)

       

      PGT-A does not diagnose any specific diseases but looks more generally at the chromosomal make-up of the embryo.

      If an embryo contains the wrong number of chromosomes (a condition known as aneuploidy), such as when one is missing, then the cells in that embryo are missing a whole set of instructions. If there is an extra chromosome, the cells will malfunction by following those instructions more often than they should. This can result in conditions such as Down syndrome.

    • Preimplantation Genetic Testing for Monogenic/Single Gene Defect (PGT-M)

       

      PGT-M is advanced single-gene testing suitable for people who have a family history of a single-gene disorder and are at risk of producing embryos affected by that condition.

      Currently PGT-M allows testing for disorders including:

      • Cystic fibrosis
      • Beta-thalassaemia
      • Thalassaemia
      • Spinal Cerebral Atrophy and Spinal Muscular Atrophy
      • BRCA1/BRCA2 (hereditary breast and/or ovarian cancer)

    Suitable for

    Before undergoing genetic testing, it’s important to know its purpose, benefits, risks, and alternatives. Even if you have no known family history of genetic disorders, general screening can offer added reassurance. Please discuss all options with your genetic counsellor or specialist. 

    To find out more about PGD, please read our fact sheet: Genetic testing 
    Have experienced recurrent miscarriage
    Have had unsuccessful IVF cycles.
    Have a family history of chromosomal disorders such as Down syndrome
    Are of an advanced maternal age (38 or over)
    Want to increase their chance of a successful IVF cycle

    The Process

    Genetic testing entails analysing an embryo’s cells to detect possible chromosomal defects. However, it is not possible to provide certainty that every disorder can be tested for. The main goal is to first determine whether the embryo is healthy and then plan the next step if anything abnormal is detected.

    The procedure follows these steps:

    Step 1: Blastocyst Culture

    Embryos are generated within an IVF cycle, using microinjection, and are grown to the blastocyst stage of development (around day 5-6).

     

    Step 2: Trophectoderm Biopsy

    Placental cells (cells from the placenta) are removed from the outer shell of the embryo via a microscopic opening made in the outer shell.

    Step 3: Cell Analysis

    The cells are then analysed to verify that all 23 pairs of chromosomes including X and Y are identified.

    Step 4: Frozen Embryo Transfer

    Generally, only one embryo is transferred (in exceptional cases two). During an FET, a cryopreserved embryo is thawed and transferred into the prepared uterus.

    Next Steps

    City Fertility have helped thousands of individuals and couples to become parents, and we would love to help you. Our fertility specialists will create a personalised treatment plan and guide you through every step of your IVF journey. With 18 IVF clinics, 50 consulting locations and over 60 specialists around Australia there is a City Fertility specialist to help you.

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    That’s why our team of specialists, scientists and nurses are here to provide personalised care and answer your questions at every stage.

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