A rare inborn error of metabolism disorder with early-onset acute encephalopathic episodes (frequently triggered by viral infections) associated with lactic acidosis and alpha-ketoglutaric aciduria which typically manifest with variable degrees of at
encéphalopathie de l'enfant par déficit en thiamine pyrophosphokinase
SNOMEDCT-BE (frequently triggered by viral infections) associated with lactic acidosis and alpha-ketoglutaric aciduria which typically manifest with variable degrees of at / 773668008
SNOMEDCT-BE (disorder) / 773668008
