Obstetrics
Gynaecology
Clinic Information
Obstetrics
Gynaecology
Clinic Information
At Sound Start, 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.
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.
2. Pregnancy Planning
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.
3. Abnormal Prenatal Test Results
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.
4. Previous Pregnancy Complications
If you have experienced pregnancy complications related to genetic conditions, such as miscarriages or stillbirths, genetic counselling can help identify potential causes and inform future pregnancies.
5. Ethnic Background
Certain genetic conditions are more common in specific ethnic groups. Genetic counselling can help assess your risk based on your ethnic background and provide recommendations for appropriate screening.
Our clinic offers a range of genetic testing options to address various concerns.
Non-Invasive Prenatal Testing (NIPT)
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.
Reproductive Carrier Screening
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.
