Neurol. praxi. 2025;26(5):386-390 | DOI: 10.36290/neu.2024.084
GBS is an autoimmune neuropathy and is the most frequent cause of acutely developed flaccid paresis. Infect or an immune impuls precede in 70 %. Molecular mimicry participates in pathogenesis. The illness developes till 4 weeks, but commonly during 2 weeks. In typical cases the GBS begins with hypesthesia and weakness of distal parts of lower etremities and then spreads in ascedent direction. Facial nerve is affected in 50 %. Paresis of ventilatory muscles may be a cause of intubation - in 30 %. Mortality undulates between 3 % and 10 %. After 6 months there are 60-80 % of patients able to walk unsupported. The relapses occure in 2-5 %. Electrophysiological investigation is very important and it defines demyelinating or axonal type of lesion. Clinical findings can be devided in generalized forms, focal forms and Miller-Fisher syndrome.
Received: November 12, 2024; Revised: December 9, 2024; Accepted: December 12, 2024; Prepublished online: December 12, 2024; Published: November 6, 2025 Show citation
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