The Angelman syndrome Clinic in Melbourne

 

The Angelman syndrome clinic is a specialist clinic jointly run by Professor Ingrid Scheffer, a world expert in epilepsy, and Dr Catherine Marraffa, a developmental paediatrician.  The clinic provides information on a range of health issues for children with Angelman syndrome in Victoria.  The specialists have an interest in global research into Angelman syndrome, and the clinic provides an opportunity to tell families and children who might be interested in participating in research in the future.

The Angelman syndrome Clinic aims to:
  

  • Ensure all the needs of the children are being met.

  • Offer advice that might include medication regimes for the treatment of epilepsy, sleep problems, and other areas of physical difficulty. 

  • Review the child’s development in self-help skills, therapy for communication skills, cognitive skills and mobility. 

  • Provide feedback to referring paediatrician regarding child’s management. 

  • Provide information to families about research programs.

Clinic Consultations
 

The clinic is run twice a year, usually in January and July, on a Monday afternoon. It is held at Specialist Clinic A1 at The Royal Children’s Hospital, Parkville. Children are only seen if already under care of a paediatrician.  Information from the child’s kindergarten, school or therapists is useful if it is available.

 

Clinic Survey

Please take the time to complete this survey if you have used the Clinic. Your answers will be of value in order to continuously improve and develop this service. Click on this link to take the survey!

To make Contact:

By referral from the child’s paediatrician. Please post to the following address:
 

Angelman syndrome Clinic
Developmental Medicine
The Royal Children’s Hospital
50 Flemington Road
Parkville
VIC 3052
 

Telephone: (03) 9345 5898

Neurodev@rch.org.au

First Point of Contact​

Contact your State Representative here

If for some reason you are unable to get through, contact our National President or National Vice President here

Visit the GiveNow Website

Our Mission

The ASAA was established to support, inform, educate, network, promote research and to advocate for families affected by Angelman syndrome - read more


© 2005 - 2018 Angelman Syndrome Association Australia. All Rights Reserved.

PROUDLY COLLABORATING WITH FAST AUSTRALIA 

FAST Australia
The Foundation for Angelman Syndrome Therapeutics Australia (FAST Australia) is an organisation of families and professionals dedicated to funding research to provide treatments that will improve the symptoms of Angelman syndrome and ultimately that will provide a cure (see website).