Rett Syndrome Study

The purposes of this study are to gain a better understanding of the disease progression of Rett syndrome and to follow the natural history of the clinical features of Rett syndrome.

Official Study Website

Rare Disease Network

Study Participation

Eligible participants include individuals at all ages who have had complete MECP2 gene analysis and have the clinical diagnosis of classic or variant Rett syndrome, with or without mutations in the gene OR individuals without clinical Rett syndrome but with MECP2 mutations.

For more information, see the Rett syndrome study fact sheet or contact This email address is being protected from spambots. You need JavaScript enabled to view it. , study coordinator.