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What is Fragile X Syndrome (FXS)?

Fragile X Syndrome (FXS) is a rare genetic disorder carried on the X chromosome that causes:

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?

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.