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SynGAP Research Fund (SRF) is a global group of families committed to accelerating the science to cure SynGAP & to supporting each other.

Our mission is to support the research and development of treatments, therapies and support systems for SynGAP1 patients worldwide.

Learn More about SYNGAP1
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Register for upcoming events!

Interpretation of SYNGAP1 Variants

Thurs., August 19th @ 10 am Pacific/1 pm Chile
Learn More
Aug 19
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Discover our latest news & updates

Does My SYNGAP1 Child Have Autism?
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Is my child’s SYNGAP1 variant going to be researched?
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2ND ANNUAL SRF SYNGAP1 SCIENTIFIC ROUND TABLE #SRFRT2
EATING WITH EMMITT.
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#SyngapCensus Q1 2021: +57 in #1Q21
762
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10 Reasons we chose #Ciitizen for the #SYNGAP1 Digital Natural History Study. #SRFdoCiitizen
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How many people have SYNGAP1? The #SyngapCensus 2Q21 says at least 808 worldwide
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SRF Grant to Boston Children's Hospital for a SYNGAP! Natural History and Biomarker Development
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Meet SYNGAP1 Patients

Rowan
Ann Arbor, Michigan
5 years old
Julia
Poland
2.5 years old
Shahy
Egypt
3 years old
Read More Stories

Knowledge Center.

SynGAP

There are 3000+ papers available on Google if you search SynGAP, 2300+ for SYNGAP1. Where to begin?

Learn More →

Epilepsy

Our patients have some specific seizures which are well described in Sheffer’s paper, above as well as this paper from German researchers, see also the video attached.

Learn More →

Ketogenic Diet

Putting a child on the powerful drugs that are used to treat our kids is not easy. As a result many parents are turning to the oldest known treatment for Epilepsy, the Ketogenic Diet. Many have had great outcomes. We urge you to learn more about it.

Learn More →
Visit Knowledge Center

SRF is phenomenal! I love how devoted they are to finding a treatment/cure for our favorite syngapians! I am blown away with this nonprofit organization and everything that they stand for. So thankful to have amazing individuals who have made it their life mission to helping our loved ones and their own!

Brittney

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