After the prodromal period, patients develop objective signs of CNS disease:
Clinical examination reveals hypereflexia, spasticity, and evidence of sympathetic overactivity indicated by pupillary dilatation and diaphoresis.
There is development of convulsions, respiratory paralysis and cardiac arrhythmias. Death usually occurs in 10-14 days from onset of neurological dysfunction if no intensive care is instituted.
Reference:
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