Visit Biobanking of Rett Syndrome and Related Disorders Website
The purpose of this study is to advance understanding of the natural history of Rett syndrome (RTT), MECP2-duplication disorder (MECP2 Dup), RTT-related disorders including CDKL5, FOXG1, and individuals with MECP2 mutations who do not have RTT. Samples with DNA will be collected.

USCF Benioff Children’s Hospital, Oakland, CA
1-925-979-4055
For study information, contact Erica Robertson [email protected].

University of California, San Diego
1-858-246-2288
For study information, contact Karen Ditslear [email protected].