What is Fragile X Syndrome (FXS)?
Fragile X Syndrome (FXS) is a rare genetic disorder carried on the X chromosome that causes:
- Intellectual disability
- Anxiety
- Behavioral challenges
- Learning challenges
- Physical characteristics (such as: longer face, larger ears, etc.)
FXS is diagnosed with a genetic blood test.
FXS affects both males and females; females often have milder symptoms than males.
Do you care for an individual ages 3 to 29 years old with the following behaviors of FXS?
- Anxiety
- Irritability
- Tantrums
- Learning challenges
If your child has FXS, a clinical trial may be an option for your family.
Now Enrolling:
Fragile X Syndrome Study (RECONNECT)
Complete the form below OR Call us at 1‑833‑680‑1155
The RECONNECT study is evaluating an investigational, topical gel to address behavioral issues related to Fragile X syndrome (FXS).
The trial is currently enrolling:
- people ages 3 to 29 with a genetic diagnosis (genetic testing may be available, if needed) of Fragile X syndrome
- who are experiencing behavioral symptoms
- and are in generally good health
Want to Learn More? Connect With Us Today!
You will receive a call back from our team after you submit the above form to discuss the RECONNECT trial, your preference to participate at a trial site OR at home and if you or your loved one are eligible to participate.
