Reye's syndrome is a very rare condition that can affect children or young adults after they've had an illness like flu or chickenpox. It can cause serious brain problems if it's not treated quickly.
Symptoms of Reye's syndrome often start 1 to 3 weeks after a child recovers from a virus like flu or chickenpox.
The child may:
Reye's syndrome most commonly affects children between 5 and 14 years of age.
Younger and older children can also sometimes get it, but it's very rare in babies under the age of 1 and in those over the age of 18.
Check symptoms on 111 online (for children aged 5 or over) or call 111 (for children under 5).
Tell the GP or person you speak to if your child has recently had an infection like flu or chickenpox and if they've taken aspirin.
If there's a chance your child might have Reye's syndrome, they'll be referred to a specialist for some tests.
Tests may include:
If your child has Reye's syndrome, they'll need to go into hospital straight away for treatment.
Treatments for Reye's syndrome may include:
Most children with Reye's syndrome make a full recovery if it's treated quickly. But some children can have long-term brain problems.
The exact cause of Reye's syndrome is unknown.
It's been linked to the use of a type of medicine known as salicylates, particularly aspirin, in young people and children under 16.
Sometimes a child with a rare genetic condition, such as medium-chain acyl-CoA dehydrogenase deficiency (MCADD), can get Reye's syndrome. This has nothing to do with the use of aspirin.
There are things you can do to reduce your child's chance of getting Reye's syndrome.
think about getting your child vaccinated against flu and other common viruses
do not give aspirin to children under the age of 16, unless their doctor prescribes it
do not give children under 16 any medicines that contain salicylic acid or salicylate, which includes some mouth ulcer gels – ask a pharmacist for advice about alternatives suitable for children