The world's largest SYNGAP1 Patient Registry and Natural History.

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.

Participants Can:

• Learn about their family member’s diagnosis

• Partner with some of the best minds in science

• Get updates on the latest research findings

• Connect with others who share their diagnosis

• Contribute to advancements that will change the future for families with SYNGAP1 gene changes.

• 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.