PPP2CA Pathways
  • Home
  • About
  • For Families
    • Join Us!
    • HJS3 Fact Sheet
    • Simons Searchlight
  • For Medical Professionals
  • Fundraising
  • More
    • Home
    • About
    • For Families
      • Join Us!
      • HJS3 Fact Sheet
      • Simons Searchlight
    • For Medical Professionals
    • Fundraising
PPP2CA Pathways
  • Home
  • About
  • For Families
    • Join Us!
    • HJS3 Fact Sheet
    • Simons Searchlight
  • For Medical Professionals
  • Fundraising

About Our Campaign and Goals

PPP2CA Pathways is a parent-led nonprofit working to accelerate research into Houge-Janssens Syndrome type 3, a rare neurodevelopmental disorder caused by changes in the PPP2CA gene. Our current campaign supports the creation of laboratory models that researchers can use to understand the disorder and test potential treatments. We aim to unite affected families, educate the medical community, and drive progress toward meaningful therapies. 

Why Research Matters

For children living with Houge-Janssens Syndrome type 3, every day brings challenges — in development, communication, movement, and health. Because this condition is so rare, it remains poorly understood, and there are no targeted treatments. Research offers the only path to answers and hope. When we invest in science, we open the door to discoveries that can change lives.

Note: PPP2CA Pathways is a fiscally sponsored project of Rare Village Foundation, a 501(c)(3) nonprofit organization. Donations are tax-deductible as allowed by law.

Copyright © 2025 PPP2CA Pathways - All Rights Reserved.

Powered by

This website uses cookies.

We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.

Accept