Reye syndrome is a rare but serious disease that most often affects children ages 6 to 12 years old. It can cause brain swelling and liver damage. It may be related to using aspirin to treat viral infections.
Reye syndrome can lead to brain damage, liver damage, and death. But if the disease is found and treated early, most children recover from Reye syndrome in a few weeks and have no lasting problems.
Reye syndrome often starts when a child is recovering from a viral illness, such as the flu or chickenpox. Symptoms usually appear 3 to 7 days after the viral illness starts. They may develop over several hours to a day or two.
The first symptoms may include:
As liver damage and brain damage get worse, other symptoms may develop, including:
If Reye syndrome is not treated quickly, it can cause death.
Your doctor will do a physical exam and ask questions about your child's symptoms, recent aspirin use, and past health problems.
Your child may need tests such as blood and urine tests, a liver biopsy, a CT scan of the head, and a lumbar puncture (spinal tap).
Reye syndrome is always treated in a hospital, often in the intensive care unit (ICU). The goal is to stop damage to the brain and liver and to prevent other problems. While in the hospital, your child will receive medicines to reduce brain swelling and will get other supportive care.
Reye syndrome can be scary for you and your child. Remember that most children recover with no problems. To help yourself and your child feel better:
Call your doctor now or seek immediate medical care if:
Watch closely for changes in your child's health, and be sure to contact your doctor if your child has any problems.
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