Multifocal Motor Neuropathy (MMN) & Immune Motor Neuropathies (IMN) 3,14
Immune/Antibody
W
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Overview
From WUSTL NeuromuscularAntibodies Clinical Electrodiagnostic Epidemiology Laboratory Pathology Treatment Variants & DDx MMN: Focal weakness Finger extension: Involvement varied MMN: Median nerve conduction block Thenar eminence: Weakness No atrophy early in disease Epidemiology Male > Female: 2-3 to 1 Prevalence: 0.29 to 1 per 100,000 (~ 5% to 10% of ALS prevalence) Drug treatment association: TNF-α antagonists, anecdotal reports Possible associated immune disorders: Ankylosing spondylitis, Crohn's disease, Celiac disease Genetics Higher frequency of homozygous SMN2 deletion (40%) than controls (10%) 17 HLA-DRB1-15:
Related Conditions
Shared genes"Classic" Guillain-Barré Syndrome
H131GD1A
Acute Immune Polyneuropathies
GD1APATHOLOGY
Acute Motor (Axonal) Neuropathy (AMAN)
IIGQ1BGM1
ACUTE NEUROPATHIES
GD1A
Antibodies vs Glycolipids & Glycoproteins
GM1MAGGQ1B
C. Anti-GM1 Antibodies
GM1IGMGM1LMN
Chronic Immune Demyelinating Neuropathies: Variants
GD1AMOTORGM1
Classification of Acute Immune Neuropathies
GD1A
External Resources
Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.