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.