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Published byVivien Whitehead Modified over 9 years ago
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Nathan McNeil, MD 4/15/2010
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1859, Landry published a report on 10 patients with an ascending paralysis Subsequently, in 1916, 3 French physicians (Guillain, Barré, and Strohl) described 2 French soldiers with motor weakness, areflexia, CSF albuminocytological dissociation, and diminished deep tendon reflexes.
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GBS is a heterogeneous grouping of immune- mediated processes generally characterized by motor, sensory, and autonomic dysfunction GBS is an acute inflammatory demyelinating polyneuropathy Symptoms Progressive symmetric ascending muscle weakness Paralysis Decreased reflexes
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Generally preceded by a bacterial or viral infection Bacterial diarrhea is frequently with Campylobacter jejuni. It’s believed that the body’s immune system creates antibodies to fight the infection that also recognize and attack the nerves— specifically Schwann cells.
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Most patients (up to 85%) with GBS achieve a full and functional recovery within 6-12 months. Recovery is maximal by 18 months Approximately 7-15% of patients have permanent neurologic sequelae including bilateral footdrop, intrinsic hand muscle wasting, sensory ataxia, and dysesthesia.
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Only plasma exchange (PE) therapy and intravenous immune serum globulin (IVIG) have proven effective for Guillain-Barré syndrome (GBS). Both have been shown to shorten recovery time by as much as 50%
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