InterRett is an international electronic, online database that allows exploration of the phenotypes associated with the variations of the MECP2 gene in Rett syndrome.
Questionnaire data includes demographic, clinical, behavioural, developmental, functional and genetic information. View latest case numbers.
Your provision of cases would be very valuable!We invite any clinicians who have cared for children or adults with Rett syndrome to participate. Data can be entered electronically through our website or by paper based questionnaires. For bulk data input we can provide a custom database. View contributing clinicians.