History
- duration of weakness (ie. hours to days to weeks/months)
- classify as rapidly progressive, acute, subacute or chronic
- mode of progression (eg. onset in arms, “ascending paralysis”)
- sensory involvement (numbness, tingling, loss of balance esp. in dark, pain/burning)
- bulbar involvement (change in voice or swallowing)
- facial weakness (trouble chewing, sucking with straw, blowing)
- extraocular muscle weakness (diplopia) or ptosis
- respiratory involvement (dyspnea, orthopnea)
- bladder or bowel involvement
- autonomic involvement (diarrhea, orthostatic dizziness, urinary retention, palpitations)
- systemic symptoms (fever, weight loss, rash, joint pain)
- recent illness or immunization (diarrheal or respiratory tract infection, oral polio vaccine)
- recent travel (out of the country, to woods [tick bites])
- precipitating factors (exertion, carbohydrate loading – with periodic paralyzes)
- fluctuation in weakness (eg. diurnal variation, fatiguability in myasthenia)
- drug or toxin exposure (canned or ‘bad’ food, pesticides, ‘statins’, lead exposure)
- family history (porphyria)
Physical Examination
Distribution and Degree of weakness
– MRC grading (0 to 5 out of 5)
– Examine extraocular muscles (? ptosis), facial muscles, neck, arms & legs
– Describe the pattern of weakness (eg.paraparesis, faciobrachial, multifocal) if possible
– Assess for fatiguability
Sensory loss
– to particular modality (vibration / proprioception vs. pain / temperature)
– is there a sensory level?
Reflexes
– are the DTRs lost (ie. areflexic), depressed preserved, or brisk
Autonomic testing
-postural vitals, abnormal sweating, pupillary response, ileus
Skin:
– the rash of Lyme disease (erythema chronicum migrans), lines on nails with arsenic poisoning (Mee’s lines), ticks, photosensitivity, Gottron’s papules (on extensor surfaces) & heliotrope discoloration over eyelids,
Spinal tenderness (with epidural abscess or hematoma, spinal tumor)
Straight leg raise (radiculopathy)
General Patterns
- Flaccid symmetric quadriparesis (+/- bulbar and respiratory involvement) with areflexia and minimal to profound sensory loss (but often sensory symptoms)- Acute neuropathy or polyradiculopathy (esp. Guillain-Barre syndrome)
- Symmetric proximal muscle weakness without sensory symptoms or signs and with preserved reflexes:- Acute myopathy (eg. polymyositis)
- Fatiguable muscle weakness with diplopia, ptosis and bulbar dysfunction- Myasthenia gravis (and other neuromuscular disorders)
- Flaccid Paraparesis with sensory level (often with reduced lower limb reflexes & bladder dysfunction)- Cauda equina syndrome
– Thoracic spinal cord lesions (eg. transverse myelitis, spinal cord infarct) - Bulbar predominant involvement- Botulism
– Myasthenia gravis
– Motor neuron diseases (ALS,)
– Pontine lesions - Ophthalmoplegia with motor weakness:- Miller-Fischer variant of GB syndrome (areflexia)
– Botulism & Tick paralysis
– Myasthenia gravis - Prominent autonomic dysfunction- Guillain-Barre syndrome
– Paraneoplastic Syndromes
– Organophosphate toxicity
– Botulism