Genetic and Rare Diseases Information Center (GARD)


Other names people use for this condition
  • Acute autoimmune peripheral neuropathy
  • GBS
  • Acute immune-mediated polyneuropathy
  • Acute inflammatory demyelinating polyneuropathy
  • Acute inflammatory demyelinating polyradiculoneuropathy
  • Acute inflammatory neuropathy
  • Acute inflammatory polyneuropathy
  • Landry-Guillain-Barre-Strohl syndrome
  • Landry's ascending paralysis
  • Post-infective polyneuritis



Guillain-Barre syndrome
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Guillain-Barre syndrome is a rare disorder in which the body's immune system attacks part of the peripheral nervous system. Symptoms of this disorder include muscle weakness, numbness, and tingling sensations, which can increase in intensity until the muscles cannot be used at all. Usually Guillain-Barre syndrome occurs a few days or weeks after a person has had symptoms of a viral infection. Occasionally, surgery or vaccinations will trigger the syndrome. It remains unclear why only some people develop Guillain-Barre syndrome. Most patients recover completely, although some continue to have some degree of weakness.[1]

References
  1. Guillain-Barré Syndrome Fact Sheet. National Institute of Neurological Disorders and Stroke Web site. September 15, 2009 Available at: http://www.ninds.nih.gov/disorders/gbs/detail_gbs.htm. Accessed November 2, 2009.

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