Pattern 1: Symmetric proximal and distal weakness with sensory loss
Pattern 2: Symmetric distal sensory loss with or without distal weakness
Consider: cryptogenic sensory polyneuropathy (CSPN)
Pattern 3: Asymmetric distal weakness with sensory loss
Pattern 4: Asymmetric proximal and distal weakness with sensory loss
Consider: polyradiculopathy or plexopathy due to diabetes mellitus,
meningeal carcinomatosis or lymphomatosis, sarcoidosis, amyloidosis, Lyme, idiopathic, hereditary
(HNPP, familial)
Pattern 5: Asymmetric distal weakness without sensory loss
Consider: A. with upper motor neuron findings motor neuron disease/ALS/PLS
B. without upper motor neuron findings
progressive muscular atrophy (PMA)
brachial amyotrophic diplegia (BAD)
leg amyotrophic diplegia (LAD)
multifocal motor neuropathy
multifocal acquired motor axonopathy (MAMA)
juvenile monomelic amyotrophy
Pattern 6: Symmetric sensory loss and distal areflexia with upper motor neuron findings
Consider: B12 deficiency and other causes of combined system degeneration with peripheral neuropathy
Copper deficiency (including Zinc toxicity)
Inherited disorders (adrenomyeloneuropathy, MLD, Friedreich’s)
Pattern 7: Symmetric weakness without sensory loss*
Consider: A. Proximal and distal weakness Spinal muscular atrophy
B. Distal weakness Hereditary motor neuropathy
Pattern 8: Focal midline proximal symmetric weakness*
Consider: Neck extensor weakness - ALS
Pattern 9: Asymmetric proprioceptive sensory loss without weakness
Consider: sensory neuronopathy (ganglionopathy) (Table 10)
Pattern 10: Autonomic Symptoms and Signs
Consider: neuropathies associated with autonomic dysfunction ( Table 7)
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