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ACUTE NEUROPATHIES

Neuropathy (Hereditary)
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Overview

From WUSTL Neuromuscular

Immune Guillain-Barré & variants Demyelinating Motor + Sensory: "Classic" Guillain-Barré Motor Sensory Axonal Motor + Sensory Motor: Associated with Infections: Campylobacter jejuni; Haemophilus influenzae Serum antibodies: IgG vs GM1 or GalNAc-GD1a gangliosides Sensory Ataxic Autonomic Cranial Nerve Syndromes Associated with serum IgG vs GQ1b ganglioside antibodies Miller-Fisher: Ataxia; Areflexia; Ophthalmoplegia Bickerstaff Brainstem Encephalitis Associated with IgG vs GT1a antibodies Pharyngo-cervico-brachial Facial diplegia Paracarcinomatous Sensory (anti-Hu) Vasculitis Chronic neuropathi

Related Conditions

Shared genes
"Classic" Guillain-Barré Syndrome
H131GD1A
Acute Immune Polyneuropathies
GD1APATHOLOGY
Acute Motor (Axonal) Neuropathy (AMAN)
IIGQ1BGM1
Antibodies vs Glycolipids & Glycoproteins
GM1MAGGQ1B
Chronic Immune Demyelinating Neuropathies: Variants
GD1AMOTORGM1
Classification of Acute Immune Neuropathies
GD1A
Demyelinating ataxic neuropathy with IgM binding to GalNAc-GD1a and GM2 gangliosides
GD1AACUTECHRONIC
Distal Motor Axonal Neuropathies: "Distal Lower Motor Neuron Syndromes"
GD1A

External Resources

WUSTL Neuromuscular
Washington University Disease Center
PubMed
Biomedical Literature
GeneReviews
NCBI Expert-Authored Reviews
Orphanet
Portal for Rare Diseases
NORD
National Organization for Rare Disorders

Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.