Treatment is very simple with those affected just needing to take biotin supplements daily – usually in the form of tablets.
Join us for our upcoming NBS forum.
When: Tuesday 30 September at 6:30pm (AEST)
Where: Online (Zoom)
Topic: Biotinidase deficiency
Featuring a panel of experts, this forum will:
Education forum
Tuesday 30 September - 6:30pm (AEST)

Ronda is a Paediatric Clinical Scientist at the Victorian Clinical Genetics Services (VCGS) and Principal Fellow in the Department of Paediatrics at the University of Melbourne.
She oversees the operation of the Victorian newborn screening program, quality improvement initiatives and implementation of new conditions.

Leniza is a Paediatric Metabolic Specialist at the Royal Children’s Hospital in Melbourne. She has been working in the field of genetics and inborn errors of metabolism since 2012.
She is passionate about improving outcomes for metabolic patients diagnosed through newborn screening.

Mercy is a Researcher/Educator at VCGS. She's a highly accomplished registered nurse with a distinguished career in clinical practice, project management, quality improvement and education.
Her diverse experience spans acute, sub-acute, and educational settings, offering a well-rounded perspective on healthcare delivery.

Holly McNamara is a registered midwife and is the NBS Educator at VCGS.
In her role, she shares her knowledge and supports healthcare professionals and organisations in providing the best care for every newborn.

The NBS laboratory operates Monday through Friday.
We are happy to answer any questions you may have about screening, delivering this service or screening results.
P 1300 118 247
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