Drago Bratkovic is a Metabolic Geneticist based in North Adelaide, at 72 King William Rd, SA 5006. He looks after people and families who are dealing with rare genetic conditions that affect how the body uses food and makes energy.
In many cases, these conditions can show up in childhood, but they can also be noticed later on. Drago often helps when there are ongoing health issues that don’t fit a simple cause. He works with families to sort through symptoms, support the right testing, and make sure results are explained in a clear way.
His care can include conditions like Pompe disease and other enzyme-related storage disorders, as well as urea cycle disorders and other metabolic problems that affect ammonia and waste removal. He also supports people with conditions such as phenylketonuria (PKU), Addison’s disease, and adrenoleukodystrophy (ALD). At times, he also helps with heart-related issues linked to inherited metabolic conditions, including cardiomyopathy.
Some conditions he sees involve muscle breakdown or energy use, like rhabdomyolysis and fatty acid oxidation disorders. Others are more to do with the immune system, blood changes, or how the nervous system develops, including different types of leukodystrophy and Leigh syndrome. There are also rarer syndromes and metabolic conditions where growth, skin, and organs can be affected, and Drago helps families understand what to watch for day to day.
Because these illnesses can be complex, Drago’s approach focuses on practical care plans that fit real life. He works closely with other specialists and the wider health team, so decisions are made together and follow the latest guidance. He also takes time to talk through what the next steps might be, including diet guidance and medical management when they are needed.
When relevant, he may discuss whether any clinical trials could be an option. He aims to keep care steady and focused, especially when families are dealing with stress and lots of appointments.
Overall, Drago Bratkovic provides support for people with inherited metabolic and genetic conditions, helping them move from confusion to clearer answers, and from answers to a workable plan.