Acute motor axonal neuropathy
AMAN is characterized by symmetric limb weakness, facial and oropharyngeal muscle weakness, areflexia, and respiratory insufficiency. A variant is AMSAN, which involves damage to axons of sensory neurons in addition to those of motor neurons and is characterized by acute onset of quadriparesis, distal sensory loss, areflexia, and respiratory insufficiency. There can also be autonomic dysfunction in both diseases. AMAN typically progresses to nadir more rapidly than AIDP.
The exact etiology is unclear, but GBS typically presents days to weeks after an infection, most commonly Campylobacter jejuni. Other reported triggers include cytomegalovirus, influenza, Epstein-Barr virus, and human immunodeficiency virus (HIV). Of note, GBS has been reported in patients with probable Zika virus infection in South America, French Polynesia, Latin America, and the Caribbean. Rarely, GBS has been associated with surgery or immunization.
AMAN occurs more frequently in China and Japan. It often progresses more rapidly than AIDP. Recovery is unpredictable; some patients recover completely in days, while others have slow and incomplete recovery.
G61.0 – Guillain-Barre syndrome
715770009 – Acute motor axonal neuropathy
- Chronic inflammatory demyelinating polyneuropathy (CIDP)
- Spinal cord compression
- Transverse myelitis
- West Nile myelitis
- Myasthenia gravis
- Amyotrophic lateral sclerosis
- Lead toxicity
- Mercury toxicity
- Organophosphate poisoning
- Porphyria (eg, acute intermittent, variegate)
- Periodic paralysis (eg, familial hypokalemic periodic paralysis)
- Tick paralysis
- Thallium toxicity
Last Updated: 03/13/2018