Clinical Manifestations
- Rapidly evolving, progressive, ascending motor paralysis with or without sensory disturbance and with areflexia
- Lower cranial nerves are frequently involved and presented with difficulty in swallowing and maintaining airway
- Bulbar involvement is most frequently manifested as B/L facial paralysis
- Fever and other constitutional symptoms are usually absent
- Diminished DTR with absent proprioception. There may be marked sensory loss
- Bladder dysfunction is late and transient.
- Deep aching pain in muscles and back
- Difficulty in swallowing due to pharyngeal muscle weakness and impaired ventilation due to intercostal muscle paralysis in 30% of cases and they require ventilatory support
- Marked autonomic dysfunction leads to Wide fluctuations in blood pressure – hypo / hyper tension, Sudden profuse diaphoresis,Peripheral vasoconstriction Resting tachycardia,Cardiac conduction abnormality, Orthostatic hypotension – severe, Thromboembolism due to immobilisation, & sudden death
- Metabolic derangements -Hyponatremia due to excessive ADH secretion


