Guillain-Barre Syndrome
Nervous System Confirmed Autoimmune

Guillain-Barre Syndrome

Also known as: GBS, Acute Inflammatory Demyelinating Polyradiculoneuropathy (AIDP), Acute polyneuropathy, Post-infectious neuropathy

Primary organ/tissue: Peripheral nervous system (nerves outside the brain and spinal cord)

Overview

Guillain-Barre Syndrome (GBS) is a rare autoimmune neurological disorder in which the body's immune system attacks the nerves outside the brain and spinal cord (peripheral nerves). This leads to muscle weakness, numbness, and sometimes paralysis, usually starting in the legs and spreading upward. Most people develop GBS after an infection, such as the flu, a stomach virus, or COVID-19. GBS is considered a medical emergency, but most people recover with proper care.

Symptoms

Tingling or numbness in the feet and hands; Muscle weakness, starting in the legs and moving upward; Difficulty walking or climbing stairs; Loss of reflexes; Difficulty breathing (in severe cases); Facial weakness or difficulty speaking/swallowing; Pain (especially in the back or limbs); Rapid progression - symptoms often worsen over days to weeks.

Causes

Believed to occur when the immune system attacks the myelin sheath or nerve axons by mistake - often after a recent illness. Common triggers include infections (Campylobacter jejuni, Influenza, Epstein-Barr virus, Zika virus, COVID-19), vaccines (rarely), or surgery/trauma.

Diagnosis

Neurological exam (to assess muscle strength and reflexes); Lumbar puncture (spinal tap) - elevated protein in cerebrospinal fluid; Electromyography (EMG) and nerve conduction studies - show slowed signals; Blood tests to rule out other causes.

Treatment

No cure, but early treatment can greatly improve outcomes: IVIG (intravenous immunoglobulin) - blocks the damaging immune response; Plasmapheresis (plasma exchange) - filters harmful antibodies from the blood; Pain relievers and supportive care; Physical therapy during recovery; Respiratory support (in severe cases requiring ventilation).

Prognosis

Most people begin to recover within 2-4 weeks after symptoms peak. 80-90% recover fully or with minor weakness. Some may have long-term nerve damage or fatigue. Recovery may take months to years. Relapses are rare but possible.

Prevalence

Affects about 1-2 in 100,000 people per year. Can occur at any age, but more common in adults over 50. Slightly more common in males.

Autoantibodies

AutoantibodyNotes
Anti-GQ1b antibodies Present in Miller Fisher syndrome variant
Anti-GM1 or GD1a antibodies Present in certain variants

Citations

  1. National Institute of Neurological Disorders and Stroke (NINDS). (2023). Guillain-Barre Syndrome Fact Sheet.
  2. CDC - Centers for Disease Control and Prevention. (2023). Guillain-Barre Syndrome (GBS) and Vaccines.
  3. Mayo Clinic. (2023). Guillain-Barre Syndrome.
  4. Yuki, N., & Hartung, H. P. (2012). Guillain-Barre syndrome. New England Journal of Medicine, 366(24), 2294-2304.