22q11.2 deletion syndrome
Information, education, community resources, and research
This section brings together plain-language information about 22q11.2 deletion syndrome, resources for people with 22q and their families, material for educators, and an archive of research activity.
Choose a route below. The information is general and educational; it is not a substitute for advice from a qualified health professional.
Understanding 22q11.2
Start with a brief introduction, then explore terminology, inheritance, and awareness.
A plain-language introduction, with links to current health information.
Terms used in this area, with a short explanation of their context.
General information about inheritance, with sources and guidance on where to seek individual advice.
A historical reflection on awareness and recognition of 22q11.2 deletion syndrome.
Families, educators, and community resources
Explore practical material for school settings and a curated directory of support and information.
Ideas for constructive communication between learners, families, and school staff.
Selected organisations and information sources for families, educators, and researchers.
Research and historical archive
These pages preserve information about earlier research planning, updates, correspondence, and events. They should be read as historical records, not as current recruitment notices or research updates.
“Small but MASSIVE” research programme
Background on the programme and its original participatory aims.
Earlier family research correspondence
Historical correspondence about an earlier research programme.