The SYNGAP1 Patient Registry collects disease-specific natural history data about individuals with SYNGAP1-related Disorders to improve the understanding of SYNGAP1-related Disorders and inform treatment development. Registry questionnaires were built from common data element standards.

SYNGAP1 Patient Registry is a research project that aims to study the SYNGAP1 gene changes that are associated with intellectual disability, epilepsy, autism, and other overlapping symptomology and neurodevelopmental disorders.

At SYNGAP1 Centers of Excellence, we’re dedicated to unraveling the mysteries of SYNGAP1-related disorders. Our multidisciplinary teams of researchers, clinicians, and caregivers collaborate to transform SYNGAP1 research into tangible solutions for patients worldwide. Together, we can make a difference!