SYNGAP1 encephalopathy is a rare genetic disorder for which there is no treatment, causing epilepsy, intellectual disability, psychomotor delay and, frequently, autism.

SYNGAP1 encephalopathy is a rare genetic disorder for which there is no treatment. It causes epilepsy, intellectual ...

The SYNGAP1 gene provides instructions for making a protein called SynGAP, which plays an essential role in nerve cells in the brain. SYNGAP1 mutations' prevalence is 2%-4% of sporadic (non-Inherited) ...

CURE SYNGAP1, the premier global patient advocacy group dedicated to transforming the lives of those living with ...

ATLANTA — June 21 is International SYNGAP1 Awareness Day, bringing awareness to a rare genetic disorder you may have never even heard of, but Atlanta parents, Suzanne and Brent Jones are working to ...

CAMP4 Therapeutics reports promising results for CMP-SYNGAP-01 and CMP-CPS-001 in treating genetic disorders, with favorable safety data. CAMP4 Therapeutics announced promising results from its ...

The Tesla Model Y features dual motors and a special wrap to bring attention to the mission to cure SYNGAP1. For those old enough to remember, the infamous Cannonball Run was more than just a wacky ...

57 hours and 56 minutes. That's how long it took three dads to drive across the country to raise money for their sons' rare genetic disease. Last week, Brett Stelmaszek, Kevin Frye and Peter ...

Five years ago, Hayden Cheng entered the world following a normal pregnancy and birth. Then her mom, Minnie Zhou, noticed her child wasn’t sleeping as a newborn should. “You know how people say, ...

The gene SYNGAP1, the variants of which are top risk factors for Autism Spectrum Disorder (ASD), has previously unappreciated effects on the developing brain, according to a new study published in ...