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GBS (Guillain-Barré syndrome) is a rare autoimmune disorder in which the immune system attacks the peripheral nerves, leading to muscle weakness and, in severe cases, paralysis.
GBS (Guillain-Barré syndrome) is a rare autoimmune disorder in which the immune system attacks the peripheral nerves, leading to muscle weakness and, in severe cases, paralysis.
Guillain-Barré syndrome (GBS) is a rare but serious autoimmune disorder affecting the peripheral nervous system. The body's immune system mistakenly attacks its own nerves, damaging the myelin sheath – the protective covering around nerve fibers – or the nerve axons themselves. This disrupts the transmission of signals between the brain and the rest of the body.
GBS affects approximately 1 to 2 people per 100,000 each year worldwide. It can occur at any age but is slightly more common in males and shows peak incidence in young adults and older individuals.
The exact cause of GBS is not fully understood. In most cases, the condition develops days to weeks after an infection that triggers an abnormal immune response. Common triggers include:
GBS typically begins with tingling and numbness in the feet or legs, which gradually spreads upward. Other symptoms include:
Symptoms typically reach their peak within 2 to 4 weeks, followed by a gradual recovery phase.
Diagnosis of GBS is based on clinical findings and supported by the following tests:
GBS is a medical emergency requiring hospitalization, often in a neurological intensive care unit. The main treatment approaches are:
After the acute phase, intensive physiotherapy and occupational therapy are essential for restoring muscle strength and function. Recovery can take months to years. Most patients recover fully or largely, though a small proportion may have lasting deficits.
The prognosis of GBS varies by individual. Approximately 80% of patients are able to walk independently within 6 months. Around 3 to 5% die from acute complications such as respiratory failure. A small percentage may develop a chronic form known as CIDP (chronic inflammatory demyelinating polyneuropathy).
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