Table 3.
The neurological manifestations of COVID-19-associated GBS
Subtype | Neuromuscular symptoms | Sensory symptoms | Autonomic dysfunction | Neurophysiological features |
---|---|---|---|---|
AIDP (65.23%) | • Ascending quadriparesis | • Anosmia and ageusia | • Voiding dysfunction | • Delayed or prolonged distal motor latencies |
• Areflexia | • Dysesthesia/paresthesia | • Constipation | • Reduced muscle action potential amplitude | |
• Impaired movement | • Vibratory and proprioceptive loss | • Respiratory failure | • Reduced motor conduction velocities | |
• Facial palsy/diplegia | • Lost light touch and pinprick sensation | • Dysphagia | • Absent sensory nerve action potentials | |
• Oropharyngeal/hypoglossal palsy | • Stocking-and-glove hypesthesia | • Irregular heartbeat | • Conduction blocks | |
• Ophthalmoparesis | • Distal allodynia | • Increased blood pressure | • Absent F waves | |
• Psychomotor agitation | • Low back and/or thoracic pain | • Multiple organ failure | • Absent H-reflex | |
• Fatigue | • Headache | • Hypotension/hypertension | • A sural sparing pattern | |
• Decreased muscle tone | • Confusion | • Brainstem and cervical meningeal enhancement | ||
• Ascending quadriplegia/paraplegia | • Dizziness | • Cranial neuritis (in nerves III, V, VI, VII, and VIII) | ||
• Loss of consciousness | • Radiculitis & plexitis on the brachial & lumbar plexus | |||
MFS (6.52%) | • Hyporeflexia or areflexia | • Anosmia and ageusia | • Dysphagia | • Enhancement with lesion of cranial nerve (CN) III |
• Ataxia | • Paresthesia | |||
• Facial palsy | • Sensory loss/numbness | |||
• Ophthalmoparesis | • Blurry vision/double vision | |||
• Oculomotor palsy | • Dizziness on walking | |||
• Pupillary dysfunction | • Headache | |||
• Eyelid ptosis | ||||
• Impaired eye movement | ||||
• Hypoglossal palsy | ||||
• Dysphonia | ||||
AIDP-MFS (6.52%) | • Overlap of AIPD & MFS symptoms | |||
AMSAN (15.23%) | • Ascending quadriparesis | • Paresthesia | • Gastroplegia | • Reduced muscle action potential amplitude |
• Quadriplegia/paraplegia | • Vibratory and Light touch loss | • Respiratory failure | • Absent sensory nerve action potential | |
• Facial paresis or palsy | • Neck or mastoid pain | • Dysphagia | • Decrease in facial nerve cMAP amplitude | |
• Areflexia | • Sensory ataxia | • Reduced sensory action potential amplitudes | ||
• Ataxia | • Reduced motor action potential amplitudes | |||
• Hypoglossal palsy | • Bilateral facial nerve enhancement | |||
• Enhanced caudal nerve roots | ||||
AMAN (2.17%) | • Progressive tetraparesis | • Tachycardia | • Reduced compound motor action potentials | |
• Tachycardia | • Absent heart rate variability | |||
• Absent heart rate variability | • Dysphagia | |||
PNC (2.17%) | • Diplopia | • Ageusia | ||
• Abducens nerve palsy | ||||
• Areflexia | ||||
FDBR*(2.17%) | • Bilateral facial nerve palsy | |||
• Unresponsive blink reflex |
AIDP acute inflammatory demyelinating polyneuropathy, AMSAN acute motor-sensory axonal neuropathy, MFS Miller-Fisher syndrome, AMAN acute motor axonal neuropathy, PNC polyneuritis cranialis, FDBR* facial diplegia without blink reflex