Friday, December 12, 2025

⚡ Motor Neuropathies

⚡ Motor Neuropathies — Complete High-Yield Overview

Motor neuropathies cause pure or predominant motor weakness due to disorders of motor axons, occasionally mimicking motor neuron disease.


🔷 1. Immune-Mediated Motor Neuropathies
  • AMAN – Acute Motor Axonal Neuropathy (GBS variant)
  • AMSAN – Motor-predominant axonal variant
  • MMN – Multifocal Motor Neuropathy (🧪 anti-GM1)
  • MADSAM – Motor-dominant Lewis–Sumner variant
  • CIDP – Motor-predominant chronic inflammatory demyelinating polyneuropathy
Autoimmune Nodopathies (Node/Paranode Antibodies)
  • Anti-NF155
  • Anti-CNTN1
  • Anti-Caspr1
Other immune causes
  • Vasculitic motor neuropathy
  • Paraneoplastic motor neuropathy:
    • Anti-Hu
    • Anti-CRMP5

🧬 2. Hereditary Motor Neuropathies
  • dHMN – Distal hereditary motor neuropathies
  • CMT Type 2 (axonal; often motor-heavy)
  • CMT X – Some variants predominantly motor
  • SMA-like hereditary motor neuropathies
  • Kennedy disease (SBMA) – Motor neuropathy + androgen receptor defect

☣️ 3. Metabolic / Toxic Motor Neuropathies
  • Porphyric neuropathy – Acute motor > sensory
  • Heavy metals: arsenic, thallium
  • Lead neuropathy – Classically causes wrist/foot drop
  • Organophosphate poisoning
  • Drug-induced motor neuropathy:
    • Vincristine
    • Paclitaxel
    • Amiodarone (rare)
    • Dapsone (rare motor)
  • Thyrotoxic neuropathy
  • Vitamin B6 toxicity (sensory ± motor)

🦠 4. Infectious Motor Neuropathies
  • Diphtheritic neuropathy (toxin-mediated; predominantly motor)
  • Poliovirus / polio-like enteroviruses
  • West Nile virus motor neuropathy
  • HIV motor axonal neuropathy
  • CMV motor polyradiculopathy (immunocompromised)
  • Zika-associated motor GBS

⚙️ 5. Motor Neuropathies Mimicking NMJ or MND

(Pure motor presentation may resemble neuropathy)

  • ALS with peripheral motor features
  • Adult SMA (Type IV)
  • PLS variants (rare LMN involvement)

🦵 6. Structural / Compressive Motor Neuropathies
  • Entrapment neuropathies (motor-predominant):
    • Ulnar neuropathy at elbow
    • Radial palsy (Saturday night palsy)
    • Common peroneal palsy
  • Traumatic nerve injury
  • Iatrogenic injury (surgery, nerve blocks)

🌐 7. Systemic / Miscellaneous Motor Neuropathies
  • Diabetic pure motor neuropathy (rare)
  • Thyroid storm–associated neuropathy
  • Critical illness polyneuropathy (motor-predominant forms)
  • Sarcoid motor neuropathy
  • Amyloidosis (motor-heavy variants)
  • Channelopathies affecting motor axonal conduction

🧠 Easy Mnemonic: “HIT MIMICS” — Causes of Motor Neuropathy

HHereditary (dHMN, CMT)
IImmune (MMN, CIDP, AMAN)
TToxic (lead, porphyria, chemotherapy)
MMetabolic (thyrotoxicosis, B6 toxicity)
IInfectious (diphtheria, polio, West Nile)
MMalignant / Paraneoplastic
CCompressive neuropathies
SSystemic (diabetes, sarcoidosis, amyloid)

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