About this study
The Global Angelman Syndrome Registry is an online patient organisation driven registry to collect information about the natural history of children and adults with Angelman Syndrome. The registry will facilitate 1) recruitment for clinical trials into therapies and interventions to benefit participants with Angelman Syndrome and their families, and 2) advancement of research and best standards of care for Angelman Syndrome.
The registry is currently available in English, Spanish, Traditional Chinese, Italian, Polish, Hindi, and Brazilian Portuguese.
Study locations
Australia
Queensland
Cairns (1)
- Foundation for Angelman Syndrome Therapeutics, Australia — Recruiting
Contact information
- Megan Tones
curator@angelmanregistry.info - Niki Armstrong
curator@angelmanregistry.info
Full registry eligibility criteria
Inclusion Criteria: * Diagnosis of Angelman Syndrome Exclusion Criteria: \-
Important information
Registry information may change. FAST context and classifications are editorial additions. Inclusion does not confirm eligibility or availability at a specific site. Review the official record and contact the study team for participation requirements.