Dr David Coman - Paediatrician, Metabolic Physician, Clinical Geneticist

He gained wide exposure to General Paediatrics, Neonatology, Clinical Genetics and Metabolic Medicine through training positions in Brisbane, Rockhampton, Melbourne, the United Kingdom and Ireland. Under the supervision of the Royal Australasian College of Physicians, David completed his General Paediatric Training in 2005 and sub-specialty training in 2006. David has an active interest in researc

h and was awarded a Masters of Philosphy from the University of Queensland in 2007. David’s area of expertise is in the diagnosis and management of children with rare diseases. A rare disease is a clinically serious disorder affecting fewer than 1 in 2000 people, and approximately 6-8% of Australians are affected by a rare disease. 80% of rare diseases are genetic, with the majority affecting children. The diagnosis of a rare disease is often delayed because of their individual small numbers and complex nature. David is a passionate rare disease advocate and engages with multiple rare disease support groups.
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David is currently involved in multiple research projects aimed at novel disease discovery, improved diagnostic testing and treatments for children with inherited genetic disorders. He is director of a national clinic for Ataxia Telangiectasia brashat.org.au and has recently been awarded a $2.5 million NHMRC research grant for a phase 2/3 trial for treatment of this disorder. He is an active research member of the Australian Genomic Health Alliance www.australiangenomics.org.au. David is actively involved in the teaching of medical students and paediatric trainees and currently holds academic appointments at The University of Queensland, Griffith University, Bond University, and Queensland University of Technology. When not working, David enjoys spending time with his family and watching as much sport as possible. He a life-long supporter of the mighty Manly Warringah Sea Eagles.