8C01.0 Acute inflammatory demyelinating polyneuropathy

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Progressive weakness of the limbs over a few days to 28 days, symmetrical deficit, areflexia, absent or mild sensory disturbance, elevated cerebrospinal fluid protein, and slowing of nerve conduction velocities are the cardinal features. The disorder may be preceded by upper respiratory or gastrointestinal infection or immunization 1 to 4 weeks prior to onset of the illness. Bifacial palsy may be present.

inclusions

• Acute Inflammatory Demyelinating Polyradiculoneuropathy

postcoordination

synonyms

• Acute inflammatory demyelinating polyneuropathy
• Guillain-Barré syndrome
• Guillain Barre syndrome
• Acute Inflammatory Demyelinating Polyradiculoneuropathy
• acute ascending paralysis
• acute encephalomyeloradiculoneuritis
• chronic polyradiculopathy
• Landry’s paralysis
• Landry’s disease
• Acute motor axonal neuropathy
• AMAN - [Acute motor axonal neuropathy]
• Acute motor sensory axonal neuropathy
• AMSAN - [Acute motor sensory axonal neuropathy]
• Acute panautonomic neuropathy
• Acute pandysautonomia
• Miller Fisher syndrome
• Bickerstaff brainstem encephalitis
• Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome
• Paraparetic variant of Guillain-Barré syndrome
• Acute sensory ataxic neuropathy

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