Our Community
As parents of children living with PPP3CA, we have found strength in coming together—supporting one another while working toward targeted, effective treatments.
If you are a parent or caregiver of someone with PPP3CA, we invite you to join our community. This includes participating in the PPP3CA registry and enrolling in Simons Searchlight (learn more here). Your involvement is critical to advancing research and bringing us closer to meaningful treatments.
When you support the PPP3CA Hope Foundation™, you’re not just making a donation—you’re standing with families, accelerating scientific discovery, and helping light the path forward for children living with rare neurodevelopmental disorders.
Because every child deserves the opportunity to thrive.
PPP3CA by the numbers:
0
Targeted treatments to date
3
Mouse models created
5
Rare disease community partnerships
5
Crystallographically derived molecular models
5
iPSC models created
13
Published papers involving PPP3CA variants
20
In at least 20 countries
100
Nearly 100 diagnosed cases
2023
PPP3CA Hope Foundation™ became a 501(c)(3) non-profit in 2023.
