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To improve the health of the community through immunisation and prevention of infectious diseases, we are conducting clinical trials of vaccines.

Our research team have done 4 studies to find out how to increase activity in children and adults with Rett syndrome.

One of the many reasons for setting up the International CDKL5 Disorder Database was to learn more about this condition.

Embrace the potential of children with Rett Syndrome by exploring how to plan opportunities for uptime, maximizing their engagement and participation in meaningful activities.

These resources include the best available evidence about the course of Rett syndrome and its management as well as practical information about family associations, specialist clinical centres and links to relevant websites.

Our Searchable online database allows you to create graphs like the one below.

Funded by the International Rett Syndrome Foundation, this international online database examines the clinical features and genetic characteristics.

With the help of clinicians and families who have children with Rett syndrome, our research aims to improve understanding of Rett syndrome.

The Australian Rett Syndrome Study is based at The Kids Research Institute Australia located in Subiaco, Western Australia. This study was established in 1993.

Using information from the Australian Rett Syndrome database, we coded symptoms according to severity scales and grouped by type and location of mutation.