AussieRett: Australian Rett Syndrome Study

AussieRett: The Australian Rett Syndrome Study is based at the Telethon Kids Institute located in Subiaco, Western Australia. This study was established in 1993 and operates in collaboration with Princess Margaret Hospital for Children, Perth and the Children's Hospital at Westmead, Sydney.

 

A unique feature of our study is that it involves all families in Australia who have a child with Rett syndrome born in or after 1976. This is in contrast to many studies overseas where only selected groups of children are involved. Being 'population-based' allows us to be confident that our research findings will be applicable to all individuals with Rett syndrome.

 

In 1999 the gene that is responsible for Rett syndrome was identified. Rett syndrome can be attributed to a mutation in the MECP2 gene (pronounced "meck-p-two"). Since then we have been working on molecular genetic studies in conjunction with Royal Perth Hospital and the Children's Hospital at Westmead.

 

MECP2

 

 

The Australian Rett Syndrome study aims:

 

  • To monitor patterns of Rett syndrome occurrence.
  • To develop and maintain an ongoing data collection which will provide information about:
    • the impact of Rett syndrome on functioning, daily living activities and health;
    • the relationship between genetic and clinical characteristics;
    • the adequacy, availability and quality of treatments and services provided;
    • the use of medical and therapeutic interventions;
    • the impact of Rett syndrome on families in terms of family functioning and support, and financial costs and resources.
  • To provide a population data source for genetic research which is a model for use elsewhere in the world.
  • To share information with medical, educational and health professionals to increase understanding about Rett syndrome.
  • To make available information which can be provided to families of newly diagnosed children to give them some expectations about their child's future.

 

 

Involvement in AussieRett

 

We liaise closely with children's specialists nationwide such as paediatricians, neurologists and geneticists as well as the national parent support organisation - the Rett Syndrome Association of Australia.

 

Referrals of children with Rett syndrome to this study come from both professionals and this parent support organisation, which has been in full support of the study since its inception. Here in Western Australia we provide opportunities for parents to meet and share experiences through education evenings and social functions. We also provide information to interested community members, health professionals and other groups such as special education teachers and therapists.

 

Dr Helen Leonard has been the Medical Director of the study since its inception in 1993. As well as overseeing the study, she has had a long-standing clinical involvement with patients through her position as a medical doctor at the Disability Services Commission. She is also involved in intellectual disability research in a joint project of Disability Services Commission, the Education Department of Western Australia and the Telethon Institute.

 

In 1995, a collaboration was established with Dr John Christodoulou, a Professor at the University of Sydney and Director of the Western Sydney Genetics program (at the Children's Hospital at Westmead). Dr Carolyn Ellaway, a Clinical Geneticist and Paediatric Specialist in the Genetic Metabolic Disorders Service at The Children's Hospital at Westmead, subsequently joined this group and Rett syndrome was the subject of her PhD thesis for which she was awarded a National Health and Medical Research scholarship.

 

The coordination of clinical assessments in Victoria is managed by Dr Gordon Baikie, a developmental paediatrican at the Royal Children's Hospital in Melbourne. Paediatric endocrinologist, Dr Helen Woodhead works at the Sydney Children's Hospital and participates in the studies relating to bone health in Rett syndrome.

 

Dr Mark Davis, manages the Neurogenetics Laboratory at Royal Perth Hospital where he is responsible for the maintenance of the DNA bank of Rett syndrome cases and their families since 1999. His laboratory is one of three genetics laboratories in Australia that are accredited to screen theMECP2gene

 

Head of Biostatistics and Genetic Epidemiology at Telethon Institute Professor Nicholas de Klerk and statisticians Peter Jacoby and Ami Bebbington provide ongoing statistical support to the project.

 

Also at the Telethon Institute, Dr Jenny Downs is a physiotherapist and researcher who has worked on many aspects of research in the Australian Rett Syndrome Study since 2005. She has a particular focus on early development, functional abilities, physical activity and scoliosis, and is a chief investigator on the current NHMRC funded study. Katherine Bathgate is a dietitian and the project coordinator for the Australian Rett Syndrome Study. She is also conducting a PhD project in the area of healthy eating and physical activity for those with Down syndrome. Alison Anderson has a background in computer science and is nearing completion of a PhD project. Alison provides important IT support to the project. Dr Kingsley Wong is a medical doctor who has an interest in research and statistical analysis. Kingsley is currently studying for a Master of Public Health degree.

 

Others who have been involved in the program are Professor Carol Bower from Telethon Institute as well as the Head of the Birth Defects Registry in WA; Professor Sue Fyfe, who is a Professor of Medical Education and previous Head of the School of Public Health at Curtin University; and Professor David Ravine is a Foundation Professor of Medical Genetics at the University of Western Australia and a Clinician at Royal Perth Hospital.

 

Dr Lakshmi Nagarajan is a paediatric neurologist at PMH whose special interests include epilepsy and sleep disorders. She is involved in the ongoing clinical component of the project as is Dr Peter Rowe and Dr Simon Williams, paediatric neurologists at PMH.

 

 

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