Last updated: Tuesday, 21, December, 2010
A rare mitochondrial disorder of acquired or genetic origin, occurring in children.
Acute onset of encephalopathy, hepatic failure and renal impairment. Bilirubin, ALT, AST, glucose; creatinine, urea, electrolytes, ammonium; blood gases; FBC.
Viral illness, especially
Particularly in association with aspirin use.See Influenza
Genetic disease, especially