About Us
About
We are a family and research-based advocacy group, working to connect the CAPRIN1 community, provide support, and power research to advance treatment options for CAPRIN1-related syndrome!
Mutations in the gene CAPRIN1 have recently been associated with a rare genetic neurodevelopmental disorder known as CAPRIN1-related syndrome in which affected individuals may have:
- Language Impairment
- Intellectual Disability
- Attention Deficit Hyperactivity Disorder (ADHD)
- Autism Spectrum Disorder (ASD)
- Seizures
- Epilepsy and other non-neurological features
Our goal is to better understand how different mutations in CAPRIN1 affect gene function and impact neurodevelopment by comparing individuals, identified through genetic testing, who have and/or carry a CAPRIN1 mutation.
Explore Genetic Discoveries
Join our mission to understand CAPRIN1 genetic mutation and its impact. Your participation can help drive vital research and awareness worldwide