Table 3

The demographic data and characteristics of AMSAN (1 case) and AMAN (1 case).

CharacteristicCase 1Case 2
Author (yr)Farah R(2005)Kraus J(2007)
PopulationIsraelCaucasian
GenderMM
Age71(AMSAN)65(AMAN)
Preceding factors++
Clinical characteristicsLimb weakness, areflexia, ptosis, dysarthria, dysphagia, respiratory failureLimb weakness, areflexia, ptosis, dysarthria, dysphagia, respiratory failure
Albumino-cytologic dissociation++
Nerve conduction++
RNS-+
Anti-AChR antibody-+
Anti-GQ1b antibody-+
Edrophonium chloride-+
Treatmentplasmapheresis, IVIGIVIG, corticosteroids, pyridostigmine, azathioprine
Thymectomy--
Prognosis62
  • M- Male, F - Female, yr - Year, MG - Myasthenia gravis, AMAN - acute motor axonal neuropathy, AMSAN - acute motor-sensory axonal neuropathy, IVIG - intravenous immunoglobulin, RNS - repetitive nerve stimulation. Functional outcome was ranked according to the adopted scale by Hughes: 0, healthy; 1, minor symptoms or signs, able to run; 2, able to walk >5 m without assistance, but unable to run; 3, able to walk >5 m with assistance; 4, bed- or chair-bound; 5, requiring assisted ventilation for at least part of the day; and 6, dead. “+” indicates the patient had precipitating factors from infectious disease.”-” indicates the patient did not have precipitating factors from infectious disease. As for the other parameters, “+” indicates positive findings, and “-” indicates negative findings