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Alternative names Return to top
Landry-Guillain-Barre syndrome; Acute idiopathic polyneuritis; Infectious polyneuritis; Acute inflammatory polyneuropathyDefinition Return to top
Guillain-Barre syndrome is a disorder caused by nerve inflammation involving progressive muscle weakness or paralysis, which often follows an infectious illness.Causes, incidence, and risk factors Return to top
Guillain-Barre syndrome is an acute type of nerve inflammation. The inflammation damages portions of the nerve cell, resulting in muscle weakness or paralysis and sensory loss. The damage usually includes loss of the myelin sheath of the nerve (demyelination), which slows the conduction of impulses through the nerve.
The damage can also cause kill the axon part of the nerve cell (denervation), which stops nerve function entirely. Without the axon, messages cannot be transferred from one nerve cell to another.
The exact cause of this disorder is unknown. It may occur at any age but is most common in people of both sexes between the ages 30 and 50. It often follows a minor infection, usually a respiratory (lung) infection or gastrointestinal (gut) infection. Frequently, signs of the original infection have disappeared before the signs of Guillain-Barre begin.
Guillain-Barre syndrome may occur in association with viral infections like mononucleosis, AIDS, and herpes simplex, or after infections with bacteria (such as mycoplasma), and some types of diarrhea. Sometimes Guillain-Barre occurs following surgery or vaccinations (such as rabies and swine flu vaccines) or in association with other medical problems such as systemic lupus erythematosus or Hodgkin's disease.
Symptoms Return to top
The disorder progresses rapidly (from days to a few weeks), causing weakness or paralysis equally on both sides of the body. As weakness starts in the legs and then spreads to the arms, it is referred to as ascending paralysis. At the same time, patients may notice tingling, foot or hand pain, and clumsiness. As paralysis worsens, the patient may require assisted ventilation in order to breathe.
The beginning phase of the illness is a rapid worsening that may take only a few hours to reach the most severe symptoms. These severe symptoms may last up to 3 weeks. This is followed by a plateau phase of no changes, then a recovery phase of improvement over days to 6 months or longer.
Typical symptoms include the following:
Signs and tests Return to top
A history of increasing muscle weakness and paralysis may indicate Guillain-Barre syndrome, especially if there was a recent illness.
Neurological examination shows muscle weakness and may indicate dysfunction of the control of involuntary (autonomic) body functions such as blood pressure and heart rate. Sensory loss may be minimal, even when sensory changes are present.
There may be evidence of decreased breathing ability caused by paralysis of the breathing muscles, and a decrease in deep tendon reflexes in the arms and legs.
Treatment Return to top
In the past, before treatment was available, many patients recovered completely with time. However, symptoms may be severe during the course of the disorder, and hospitalization is usually required to support breathing function and prevent complications and to provide physical therapy.Support Groups Return to top
Guillain-Barre Syndrome Foundation International
Expectations (prognosis) Return to top
Almost all cases (95%) survive and the majority recover completely. Mild weakness may persist for some people. The outcome is most likely to be very good when symptoms remit within 3 weeks of their onset.Complications Return to top
Calling your health care provider Return to top
Go to the emergency room or call the local emergency number (such as 911) if loss of movement, decreased sensation or other emergency symptoms occur, including difficulty swallowing or breathing, feeling "unable to take a deep breath," or fainting. Update Date: 4/25/2004 Updated by: Joseph V. Campellone, M.D., Division of Neurology, Cooper University Hospital, Camden, NJ. Review provided by VeriMed Healthcare Network.
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Page last updated: 28 October 2004 |