Advancing Treatment, Improving Lives
Funding research to impact treatment
The FOXP1 Medical Research Foundation is committed to advancing rigorous, innovative medical research to discover treatments—and ultimately a cure—for FOXP1 syndrome.
We fund and support scientific studies, foster collaboration among researchers, clinicians, and families, and advocate for faster pathways from discovery to therapy.
There are currently no therapeutics to treat FOXP1 Syndrome. Our goal is to improve quality of life and long-term outcomes for all individuals affected by this rare neurodevelopmental disorder.
“Being told there is nothing we can do for our children is unacceptable.”
— FOXP1 Parent
A rare neurodevelopmental genetic condition
Almost all individuals with FOXP1 Syndrome have delays in speech, language and overall development. They also may experience a wide range of other physical difficulties. With the right therapies and support, many individuals make important progress and improve their quality of life.
Potential symptoms of FOXP1 Syndrome include:
Brain
Speech
Intellectual Disability
Autism
Sleep
Anxiety
Seizures
Body
Motor Delays / Low Tone
Hearing / Vision
Feeding
Heart
Kidney
Immune System
Leadership
We are FOXP1 parents with experience in healthcare and research
Dr. Samit Dasgupta
Mikhal Roman
Advisory Board
We are scientists, doctors, and industry experts
Dr. Wendy Chung
Dr. Simon Fisher
Dr. Genevieve Konopka
Dr. Siddharth Srivastava
Dr. Sharyl Fyffe-Maricich
Dr. Rachel Groth
“The science is at a place where life-changing treatments are within reach for our children.”
— Rare Disease Parent / Industry Expert
What to expect next
We’ll be sharing a wealth of new content and resources to keep you informed and involved. Be sure to sign up for our email list so you don’t miss the latest updates.
Here’s a preview of what’s ahead:
Research Roadmap
A clear framework outlining how we’re investing in research.
Treatment Development
An inside look at the types of therapies we’re exploring.
FOXP1 Science Made Simple
Easy-to-understand explanations of the science behind FOXP1 Syndrome and what it means for potential treatments.
Resources for Families & Caregivers
Therapeutic tools, medical information, and support materials.
Opportunities to Participate
Learn how you can get involved in scientific studies.
Fundraising Initiatives
Ways to support our mission and accelerate progress.
Let us know what is most interesting to you in the form below.
Stay informed about advances in FOXP1 Medical Research
For additional resources, please visit our friends at the International FOXP1 Foundation