Genetic screening provides insight into inherited conditions that may affect your pregnancy or your child's health. Understanding your results early gives you the information you need to make considered decisions about your care and your family's future.
Carrier screening identifies whether you or your partner carries gene variants associated with inherited conditions that could be passed on to your child. It is available before conception and during early pregnancy, and is recommended for all couples planning a pregnancy regardless of family history. Our GPs can organise screening and walk you through what the results mean for your situation.
Prenatal genetic testing, including Non-Invasive Prenatal Testing (NIPT), provides information about your baby's chromosomal health during pregnancy. We offer guidance on the options available, what each test involves and what to expect from your results, so you can make informed decisions at each stage.
A positive or unexpected result can feel overwhelming. Our GPs take the time to explain what your results mean in plain language, discuss your options and connect you with the right support where needed. You’ll never be left to navigate that on your own.
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