"It's a slow-moving train wreck," Mike Graglia says about his 12-year-old son Tony's rare genetic disease with no cure. Caused by a tiny fluke of nature—a mutation in a gene known as a SYNGAP1—the non ...
Mill Valley, CA – February 11, 2025 – The SynGAP Research Fund 501(c)(3) dba Cure SYNGAP1 proudly announces the release of its inaugural Impact Report, a transparent and celebratory reporting of ...
synapses, which plays a key role in regulating synaptic strength and plasticity—both essential for learning and memory. Disruptions in SYNGAP1 protein levels lead to the cognitive and developmental ...
Children born with a damaged gene needed for healthy brain development, SYNGAP1, experience seizures, sensory processing disorders, difficulty speaking, intellectual disability, and autism-like ...
A single microscopic change in our DNA can permanently alter how the brain is built, locking in developmental problems that no amount of later effort can fully undo. Researchers are now tracing how ...
The mechanisms underlying intellectual disabilities or autism remain largely unknown. Researchers in the labs of Prof. Pierre Vanderhaeghen and Prof. Vincent Bonin at the VIB-KU Leuven Center for ...
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 ...
Becky Quick outlines her daughter's personal struggle with SYNGAP1. Quick explains why her daughter's journey inspired her to launch CNBC Cures. I've spent the last 25 years in front of the camera ...
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