- characterized by acute noninflammatory encephalopathy and hepatic failure
- the etiology of Reye syndrome is unknown , occurs after a viral illness, particularly an upper respiratory tract infection (URTI), influenza, varicella, or gastroenteritis, and it is associated with the use of aspirin during the illness.
- more than 3-fold increase in alanine aminotransferase (ALT), aspartate aminotransferase (AST), and/or ammonia levels
- Inborn errors that may mimic Reye syndrome include fatty-acid oxidation defects, amino and organic acidopathies, urea-cycle defects, and disorders of carbohydrate metabolism
- Reye syndrome is equally distributed between the sexes.
- Reye syndrome rarely occurs in newborns or in children older than 18 years
- Reye syndrome can occur after vaccination with live viral vaccines.
- Clinical features : pernicious vomiting Lethargy Diarrhea and hyperventilation
- No specific treatment exists. Continue careful monitoring.
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