Trial Number

700-10

Age range

All ages

Gender

Male or Female

Enrolling Patients

Yes

Fragile X syndrome (FX) is a condition that arises due to a genetic mutation on the human X chromosome and is associated with different degrees of intellectual impairment, autism, speech delays and learning disabilities. The severity of the associated abnormalities depends on how severe the mutation is. The Fragile X Clinical and Research Consortium (FXCRC) is a collaborative endeavor initiated in 2006 by the National Fragile X Foundation (NFXF) to advance clinical practice and facilitate coordinated, collaborative multi-site research on Fragile X syndrome. This project will establish standards of care, facilitate the conduct of multi-institutional clinical research projects, coordinate and organize research across sites, build a reliable, dynamic patient registry and assist member clinics in data collection and analysis, including effective and relevant outreach and surveillance.

Principal Investigator

MemorialCare Research Center Contact Form

For further information about this study or to express your interest in this study, please fill out and submit this form.

Name
Address
Enter Trial number from the area just below the marquee.
How would you prefer to be contacted?
How did you hear about us?
This registration is for:
CAPTCHA This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.