Neurogenetics
Expert guidance for individuals and families navigating neurological conditions with a genetic basis.
At Rosalind Genetics, we provide specialist assessment, counselling, and testing for a wide range of inherited neurological conditions. Our neurogenetics service helps uncover the genetic causes of conditions that affect movement, cognition, muscle function, and the nervous system – offering clarity, support, and options for families and clinicians.
When should I consider neurogenetic services?
Some neurological conditions are caused by changes in our genes – these can affect both children and adults, and may involve muscle strength, movement, memory, development, or behaviour. Genetic testing can help explain why a condition has occurred, guide treatment, and support family planning.
You may benefit from neurogenetic services if you or someone in your family has:
Unexplained muscle weakness or motor difficulties
Progressive neurological symptoms (e.g. tremor, ataxia, spasticity, seizures)
Developmental delay, intellectual disability or autism
Epilepsy (particularly early-onset, treatment-resistant or syndromic forms)
A known or suspected neurogenetic condition (e.g. Huntington disease, muscular dystrophy, Rett syndrome)
A family history of inherited neurological or neuromuscular conditions
What to expect
Every case is unique. We take the time to tailor your care to your situation.
1
Referral
Get a referral from your GP to Rosalind Genetics.
2
Consult
Speak to our genetic counselling team about your options in a telehealth consult online.
3
Family History
Discuss your family history and whether testing is appropriate.
4
Undergo testing
Undertake testing (if needed). We’ll explain what it covers and what results mean.
5
Results
Receive your results with clear guidance and emotional support.
6
Next steps
Follow-up support, including referrals, family testing, and care coordination.
1. Get a referral
From your GP, obstetrician, or fertility specialist.
2. Consultation
Meet with one of our genetic counsellors (in person or via telehealth).
3. Family history
Discuss your family history and whether testing is appropriate.
4. Undertake testing
Undertake testing (if needed). We’ll explain what it covers and what results mean.
5. Results
Receive your results with clear guidance and emotional support.
6. Next steps
Plan your next steps with confidence, whatever the outcome.
What conditions do we support?
We assess and advise on a wide range of neurological and neuromuscular conditions, including:
- Neuromuscular disorders (e.g. muscular dystrophy, Charcot-Marie-Tooth, spinal muscular atrophy)
- Neurodevelopmental disorders (e.g. intellectual disability, autism, Rett syndrome)
- Movement disorders (e.g. ataxia, dystonia, early-onset Parkinson’s disease)
- Epilepsy syndromes (particularly early-onset or treatment-resistant forms)
- Neurodegenerative conditions (e.g. Huntington disease, leukodystrophies)
- Peripheral nerve disorders and mitochondrial conditions
Genetic testing may not always provide a clear-cut diagnosis, but it can offer direction for care, connect you with support, and inform decisions about family planning.
Medicare and costs
Many neurogenetic tests are eligible for Medicare rebates, particularly when there is a strong clinical or family history.
We’ll talk you through all costs before testing – there are no hidden fees, and you’re never obligated to proceed.
Why Choose Rosalind?
Rosalind’s team includes clinical geneticists and counsellors with deep expertise who work closely with neurologists, paediatricians, allied health teams and diagnostic labs across Australia.
We offer:
- Care that’s collaborative and patient-centred
- Support for both diagnosis and long-term planning
- Coordination of family testing and specialist referrals
We know these journeys are complex. You’re not expected to navigate them alone.
Frequently Asked Questions
Do I need a referral?
Yes. You’ll need a referral from a GP or specialist to access this genetic testing service.
Will testing lead to a diagnosis?
Sometimes – but not always. Even when results are uncertain, testing can still help rule things out or guide future care.
What if my child has already had testing elsewhere?
We can review existing results and help determine if additional testing is appropriate.
Can other family members be tested?
Yes – if a gene change is found, we can offer testing and counselling to other relatives as needed.
How long do results take?
It depends on the type of test. Most results are available within 4 to 8 weeks. We’ll explain the timeline during your consultation.
Have more questions?
Reach out to us at gene@rosalindgenetics.com or call us on 1300 042 132.