Research Participant Registry Core

The goal of the study is to learn more about the early brain and behavioral development of infants with fragile X syndrome to aid in the future development of supports and treatments.

Infants 6 months and under with a fragile X full mutation. Travel expenses to UNC-Chapel Hill are paid and families will be compensated $200. There is a follow up visit at 24 months. Contact: Julia_gross@med.unc.edu