Genetic Counselling
We offer comprehensive genetic counselling services to support individuals and families in understanding and managing genetic health risks.
Our experienced team of genetic counsellors provide personalised guidance on a range of genetic testing options, including Non-Invasive Prenatal Testing (NIPT) and Reproductive Carrier Screening. Our aim is to empower you with the information needed to make informed decisions about your reproductive health. Our genetic counsellors work closely with you to ensure you have a clear understanding of your options and the potential outcomes of genetic testing
There are several reasons why you might seek genetic counselling
If you have a family history of genetic conditions, such as cystic fibrosis or muscular dystrophy, genetic counselling can help you understand the likelihood of these conditions being passed on to your children.
Couples planning a pregnancy can benefit from genetic counselling to assess their risk of passing on genetic disorders. This can provide peace of mind and help with family planning decisions.
If you receive abnormal results from prenatal screening tests, genetic counselling can provide clarity and guidance on the next steps. Our counsellors can help you understand the implications of these results and explore further testing options.
Our clinic offers a range of genetic testing options to address various concerns.
NIPT is a safe and effective screening method for detecting chromosomal abnormalities in a developing foetus. This test analyses cell-free foetal DNA in the mother’s blood to assess the risk of conditions such as Down syndrome, trisomy 18, and trisomy 13.
This type of screening identifies carriers of genetic conditions that could be passed on to offspring. It is recommended for couples planning a pregnancy or those undergoing assisted reproductive technologies. Carrier screening can detect conditions such as cystic fibrosis, spinal muscular atrophy, and fragile X syndrome, providing valuable information for family planning.
Our genetic counsellors take the time to understand your unique situation, answer your questions, and provide the support you need. We work closely with other healthcare providers to ensure coordinated care and the best possible outcomes for you and your family.
Our state-of-the-art facility is equipped with the latest technology to offer accurate and reliable testing. We prioritise your privacy and ensure that all consultations are conducted in a confidential and supportive environment.
Non-invasive prenatal testing (NIPT) is the most widely requested form of early pregnancy screening used to check for trisomy 21 (Down syndrome) and other common chromosomal aneuploidies.
Another important way to screen for chromosomal aneuploidies is through the combined First Trimester Screen (FTS), previously known as the Nuchal Translucency scan. If you decide to have NIPT, CFTS is still important for other valuable information.
Bundle Inclusions
- Genetic Counselling by our Genetic Counsellor
- Viability Scan approx. 10 weeks’
- Genetic Carrier Screening
- First Trimester Nuchal Bloods
- Pre-Eclampsia (blood pressure) Screening
- NIPT^
- Early Anatomy Scan
- Scans completed, and reported on by Intuition’s Maternal Fetal Medicine Specialist
Get in touch
If you wish to make a booking with one of our specialists or allied health team, please get in touch with our friendly support staff.
We understand the need for women-led care and have an easy referral system to other health care professionals who provide a range of services specialised to your individual needs.
