Facing a possible genetic condition can feel overwhelming. whether for you, your child, or your future family, You may be searching for answers, reassurance, or a plan for moving forward. That’s where we come in.

At our clinic, we provide compassionate, personalized care to help individuals and families understand their genetic health. We work with children, adults and couples who have:

• Developmental delays, learning difficulties, or intellectual disabilities
• Genetic syndromes affecting health, growth, or development
• Ultrasound abnormalities in a baby

• Birth defects or congenital malformations
• A family history of inherited conditions
• Neurological, cardiac, renal disorders (in fact, disorders affecting any organ system)
• Sensory abnormalities (e.g. affecting hearing & vision)
• Unexplained medical concerns that may have a genetic basis
• Reproductive and fertility issues – see below for more
• Cancer genetics – we provide advice on cancer genetics and genetic testing for known genetic mutations in your family. For more detailed cancer screening and monitoring we suggest you seek the advice of a cancer geneticist.

For couples hoping to start or grow their family, genetics can be a vital piece of the puzzle. If you’re navigating fertility challenges, pregnancy loss, or concerns about passing on a condition, we can offer clarity and guidance.
We provide:

• Preconception genetic counselling – Helping you understand potential risks before pregnancy
• Carrier screening – Checking for inherited conditions that could affect your child
• Support for recurrent miscarriage – Investigating whether genetics play a role
• IVF and genetic testing advice – Helping you make informed choices
• Prenatal genetic assessments – Understanding conditions that may affect your baby before birth

Whatever brings you to our clinic, we want you to know this: you are not alone. We take the time to listen, explain, and support you through each step.