The largest SYNGAP1 Patient Registry and Natural History in the World

SYNGAP1(MRD5) Natural History Study and Registry is a research project that aims to study the SYNGAP1gene 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(MRD5) Natural History Study and Registry is a research project that aims to study the SYNGAP1gene changes that are associated with intellectual disability, epilepsy, autism, and other overlapping symptomology and neurodevelopmental disorders.