Reye's Syndrome
Reye's Syndrome Reye's Syndrome is a rare but serious condition that causes swelling in the liver and brain. It most commonly affects children and teenagers recovering from a viral infection, most often the flu or chickenpox. Early diagnosis and treatment are crucial to prevent serious complications or death.
Symptoms[edit | edit source]
The symptoms of Reye's Syndrome typically appear after a viral infection has started to improve. They can include:
- Persistent vomiting
- Lethargy or drowsiness
- Irritability or aggressive behavior
- Confusion or hallucinations
- Weakness or paralysis in the arms and legs
- Seizures
- Decreased level of consciousness
Causes[edit | edit source]
The exact cause of Reye's Syndrome is unknown, but it has been associated with the use of aspirin to treat viral illnesses in children and teenagers. It is believed that aspirin may trigger Reye's Syndrome in individuals who have an underlying metabolic condition.
Diagnosis[edit | edit source]
Diagnosing Reye's Syndrome involves:
- A thorough medical history and physical examination
- Blood tests to check liver function and ammonia levels
- Imaging studies such as a CT scan or MRI to assess brain swelling
- A liver biopsy may be performed to confirm the diagnosis
Treatment[edit | edit source]
There is no specific cure for Reye's Syndrome, but supportive care in a hospital setting is essential. Treatment focuses on:
- Reducing brain swelling
- Preventing complications
- Supporting vital organ functions
Medications may include:
- Intravenous fluids
- Electrolytes
- Diuretics to reduce fluid buildup
- Medications to control seizures
Prevention[edit | edit source]
The best way to prevent Reye's Syndrome is to avoid giving aspirin to children and teenagers recovering from viral infections. Instead, use alternative medications such as acetaminophen or ibuprofen for fever and pain relief.
Prognosis[edit | edit source]
The prognosis for Reye's Syndrome varies. Early diagnosis and treatment improve the chances of recovery. However, severe cases can lead to permanent brain damage or death.
History[edit | edit source]
Reye's Syndrome was first described in 1963 by Dr. R. Douglas Reye, an Australian pathologist. Since then, awareness and preventive measures have significantly reduced the incidence of the disease.
See Also[edit | edit source]
- Aspirin
- Viral Infections
- Liver Function Tests
- National Institute of Neurological Disorders and Stroke. "Reye's Syndrome Information Page."
- Centers for Disease Control and Prevention. "Reye's Syndrome."
External Links[edit | edit source]
NIH genetic and rare disease info[edit source]
Reye's Syndrome is a rare disease.
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Contributors: Prab R. Tumpati, MD