Abstract
Acute immune-mediated peripheral nerve system dysfunction known as Guillain-Barre Syndrome (GBS) is typified by rapidly worsening muscle weakness, which frequently begins in the lower limbs and can eventually result in paralysis. It is typically brought on by an infectious event, most often a bacterial or viral infection, with Campylobacter jejuni being the most often linked harmful organism. According to epidemiology, there are 1-2 instances of GBS for every 100,000 people each year, with a small male predominance and greater frequency in adults over 50. Nerve conduction investigations and cerebrospinal fluid analysis demonstrating albumin cytological separation complement the largely clinical diagnosis.
Published Version
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