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A Night of Impact for Cure SYNGAP1 💙 My nephew Greyson was diagnosed with SYNGAP1 at just 20 months old, and it has forever changed our family’s lives. SYNGAP1 is caused by a mutation on the SYNGAP1 gene, leading to a lack of SYNGAP protein, which is essential for proper brain function. This night meant so much to us as we came together to raise money and awareness in hopes of finding a cure. A cure for Greyson would mean the world to our family. It would allow us deeper into his world and help
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