PTLS Hope Research Foundation

These aren’t just photos.
They are the reason the research matters.

Every face in this carousel represents a child living with Potocki-Lupski Syndrome and a future we are working to change through advanced genetic research, deep RNA analysis, and AI-driven discovery.

This community is not waiting.
We are mapping biology.
We are funding breakthroughs.
We are building the data our researchers need to move closer to treatment.

This is personal.
This is urgent.
This is possible.

Please make a meaningful donation to fuel our research pipeline.

New diagnosis? Feeling overwhelmed?

The best place to start is with community.

Our global PTLS Parent Support Group run by has been active for over 14 years sharing therapy insights, school advice, medical experiences, and real-life support.

It’s where families find answers faster.

It’s where no one feels alone.

Join us, link in bio.