What is the potential for genomics in everyday healthcare?

Making an earlier, more accurate diagnosis

At the age of only nine months, Laura had a urinary tract infection. This led to an ultrasound that showed 'bright' kidneys. Laura was referred to a paediatric nephrologist and had many tests, without a clear answer to explain the abnormal appearance of her kidneys.

Helping guide patient care

Michael was diagnosed with terminal cancer. Genomic sequencing through Melbourne Genomics changed his diagnosis, his treatment, and his life.

Providing families with answers

Tyler and Hayden Smith are brothers whose lives have been transformed by genomics. Both experienced severe unexplained illness since birth, including Crohn’s disease, inflammatory bowel disorder, and respiratory tract infections, among other problems.

Can I have a genomic test?

As of 1 May 2020, genomic testing to diagnose children with a suspected complex genetic condition is funded by Medicare. Findings from Melbourne Genomics clinical projects were instrumental in making the case for this new Medicare funding (which was carried forward by the aligned national alliance, Australian Genomics).

Any questions you have about genomic testing should be discussed with your medical specialists.

More information about genetic and genomic testing in Victoria is available here.

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Melbourne Genomics acknowledges the Wurundjeri people of the Kulin Nation, on whose lands we work, and all First Nations peoples across Victoria. We pay respect to Elders past and present. We also acknowledge the First Nations health professionals, researchers and leaders who are shaping the future of genomic medicine.

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