peripheral neuropathy patterns Flashcards
Pattern 1: Symmetric proximal and distal weakness with sensory loss
Consider: inflammatory demyelinating polyneuropathy (GBS and CIDP)
Pattern 2: Symmetric distal sensory loss with or without distal weakness
Consider: cryptogenic sensory polyneuropathy (CSPN)
metabolic disorders
drugs, toxins
hereditary (Charcot-Marie-Tooth, amyloidosis and others)
Pattern 3: Asymmetric distal weakness with sensory loss
Multiple nerves, consider: vasculitis
hereditary neuropathy with liability to pressure palsies (HNPP)
multifocal acquired demyelinating sensory and motor (MADSAM) neuropathy infectious (leprosy, lyme, sarcoid, HIV)
Single nerves/regions, consider: compressive mononeuropathy and radiculopathy
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)
a. brachial amyotrophic diplegia (BAD)
b. 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
1. Spinal muscular atrophy
B. Distal weakness
1. Hereditary motor neuropathy
Pattern 8: Focal midline proximal symmetric weakness*
Consider: Neck extensor weakness - ALS
Bulbar weakness - ALS, PLS
Pattern 9: Asymmetric proprioceptive sensory loss without weakness
Consider: sensory neuronopathy (ganglionopathy) (Table 10) chronic immune sensory polyradiculopathy (CISP)
Pattern 10: Autonomic Symptoms and Signs
Consider: neuropathies associated with autonomic dysfunction (Table 7)
Hereditary sensory autonomic neuropathy Diabetes mellitus
Amyloidosis (familial and acquired) Guillain-Barre syndrome
Vincristine induced
Porphyria
HIV-related autonomic neuropathy Idiopathic pandysautonomia