Neuromuscular HOMEepAGE

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Specific associated clinical syndromes

Immune/Antibody

View full entry on WUSTL Neuromuscular

antibody/mprotein.htm#specific

Overview

From WUSTL Neuromuscular

Amyloidosis IgA Cryoglobulinemia IgG & IgA MGUS Neuropathy May progress to Multiple myeloma Other plasma cell neoplasms IgM MGUS: Syndromes 13 General MYD88 L265P mutations may be more common that IgM MGUS without related disease Syndromes related to antigenic target of IgM antibody Decorin (BJ): Myopathy GALOP antigen: Gait disorder & polyneuropathy GD1b ganglioside (without GM1 binding): Ataxic sensory neuropathy; Ophthalmoplegia GM1 ganglioside: Motor neuropathy GM2/GalNAc-GD1a ganglioside: Demyelinating, Sensory neuropathy Myelin-associated glycoprotein (MAG): Sensory ± Motor neuropathy; G

Related Conditions

Shared genes

"Classic" Guillain-Barré Syndrome

Acute Immune Polyneuropathies

Acute Motor (Axonal) Neuropathy (AMAN)

ACUTE NEUROPATHIES

Antibodies vs Glycolipids & Glycoproteins

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

HDSDISACCHARIDEMAG

Chronic Immune Demyelinating Neuropathies: Variants

CHRONIC IMMUNE POLYNEUROPATHIES: AXONAL

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.