There is currently no cure for DiGeorge syndrome. But support is available.
Children and adults with the condition have regular check-ups for any problems. They can get treatment, if needed.
For example, someone with DiGeorge syndrome may have:
- regular hearing tests and blood tests
- heart scans
- blood pressure checks
- measurements of their height and weight
- an assessment before they start school to see what supports they need
- regular dental check-ups throughout childhood
- hearing and vision checks once or twice a year
- speech and language therapy to help with communicating
- changes to their diet or a temporary feeding tube to help with feeding problems
- physiotherapy for problems with strength and mobility
- treatment from a podiatrist for foot and leg problems
- shoe inserts (orthoses) for leg pain
- surgery (an operation) for severe problems such as heart conditions or a cleft palate
Some people will need:
- extra booster vaccines to protect against infections
- vitamin D supplements, such as multivitamins
- fish oil supplements
- help managing constipation from a GP or paediatrician
All children will need an ultrasound scan of their kidneys following diagnosis.
A spinal x-ray is also recommended while the child is able to stand well. They usually have this before starting school.
More support
You may find it useful to talk to a social worker, psychologist or counsellor. You can contact these directly, or ask your GP or care team to refer you.
You can also get support from the charity 22q11 Ireland.