Phenylketonuria also called PKU, is a rare inherited disorder that causes an amino acid called phenylalanine to build up in the body. PKU is caused by a change in the phenylalanine hydroxylase (PAH) gene. This gene helps create the enzyme needed to break down phenylalanine.
I have always been passionate about making a difference in the lives of people living with chronic disease, and I feel the best way of doing so is through research. Over the past 5 years, I have pursued a career in scientific research, developing my knowledge and skills as a scientist and researcher.
Growing up in regional Victoria, the opportunities to explore science is limited. The first science program I was involved in was the Rotary’s National Youth Science Forum. In my last year of high school, I was accepted to take part in the National Youth Science Forum, participating in the Brisbane session at the University of Queensland.
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