Paediatric whole exome sequencing
Want access to ~$3,000 worth of Medicare funded testing?*
Rare genetic conditions and complex paediatric cases are our specialty and we want to shorten the odyssey between onset and diagnosis.
Did you know it can take between 7 and 10 years for a rare condition to be diagnosed? So here at Genomic Health we are doing our bit to help families to hopefully halve their diagnostic odyssey.
80% of rare conditions are genetic
We offer Paediatric whole exome sequencing (WES) that is Medicare funded for children under 11 years of age*.
Older than 11 years? There is a self funded option we can discuss with you.
In consultation with our Clinical Geneticist and Genetic Counsellor, we help families understand what this means and why it might be useful and more importantly, what the results are going to show.
We can do this quickly and easily with access to no wait times for appointments and fast result turnaround time of ~10 weeks and best of all - its free under Medicare*.
Get in touch to find out more with an
Health Care Professionals refer here
both parents must be referred
In depth genetic testing for your child
“I would like to thank you and your company for helping me out and it’s wonderful that we can access these services privately. I really don't think I would have had any chance at all of finding out about this condition otherwise.” - AS
*qualifying criteria exists and consult fees apply