The purpose of Syngap research is to enable and promote efficient research projects into SynGAP. We are striving for a cure for our kids, the SynGAP community and other genetic epilepsies.

Syngap research is raising funds for research into a genetic disorder that can cause severe epilepsy, intellectual disability, and autism.

The first research project is through the Florey Institute to research Syngap1 via:

  • Generation of patient-derived stem cell model

  • Drug screen and ASO strategy

The long term goal for SynGAP research is to help fund the creation of a precision medicine hub in Australia focused on finding a cure for genetic epilepsies

SynGAP is widely considered a disease gene. Scientists believe that understanding the SynGAP mechanism and how to correct it will provide crucial insights for other genetic conditions like Intellectual disability, epilepsy and autism.

The role of SYNGAP1 is to give the instructions for the production of a protein called SynGAP, which generally suppresses the level of brain activity. When there is not enough SYNGAP1, the brain is generally more excitable. This explains why individuals with changes in the SYNGAP1 gene have the problems they do, especially in the areas of learning, seizures, hyperactivity and sleep disturbance. 

For more information, visit:

https://www.facebook.com/Syngapresearch/

Epilepsy Foundation

Every day we try to make life better for people living with epilepsy and this is made possible because of the support of people like you. The Epilepsy Foundation encourages the community to get involved with fundraising so people living with epilepsy don’t have to go it alone.

Our services include information, advice and support, epilepsy counselling, case management and practical assistance, as well as education and training, social and psychological research and advocacy for and with people with epilepsy.

5 heroes fundraising today.


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