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CHRONIC IMMUNE POLYNEUROPATHIES: AXONAL

Immune/Antibody

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Overview

From WUSTL Neuromuscular

Amyloidosis Ataxic Sensory + GD1b antibodies Distal lower motor neuron syndromes Distal sensory FGFR-3 Perineuritis Sensory + NF-H antibody Sulfatide antibody-related Systemic Immune/Vasculitis ADA2 deficiency EGPA PAN Rheumatoid Arthritis SLE SSc Trigeminal sensory TS-HDS antibody Vasculitic neuropathies Also see: Acute motor axonal neuropathy Sensory neuronopathies Duchenne

Related Conditions

Shared genes

Axonal Sensory Neuropathies with Serum IgM binding to Trisulfated Heparin Disaccharide (TS-HDS)

HDSDISACCHARIDEMAG

Monoclonal Gammopathies of Unknown Significance (& Other)

Neuropathy with IgM binding to Myelin-Associated Glycoprotein (MAG)

MAGHDSPHOSPHACAN

Other Muscle Features

VAMPINCLUSIONBCIM

Rituximab Infusion Protocol

Sensory Neuronopathies

Specific associated clinical syndromes

External Resources

WUSTL Neuromuscular

Washington University Disease Center

Biomedical Literature

NCBI Expert-Authored Reviews

Portal for Rare Diseases

National Organization for Rare Disorders

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