Rett syndrome is a rare neurological disorder mainly affecting females. We manage two databases that collect information from families and clinicians to better understand the course of Rett syndrome and effectiveness of treatments.
Read about an Australian campaign to raise awareness and vital funds for MECP2 duplication syndrome research.
InterRett was established in 2002 and collects information about children and adults with Rett syndrome of any age from around the world.
Registration and questionnaire are also available in the following languages:
To generate graphs from our InterRett data search our database!
View a brochure about InterRett.