Copyright
©The Author(s) 2017.
World J Clin Cases. Jul 16, 2017; 5(7): 270-279
Published online Jul 16, 2017. doi: 10.12998/wjcc.v5.i7.270
Published online Jul 16, 2017. doi: 10.12998/wjcc.v5.i7.270
Features required for diagnosis |
Progressive weakness in both arms and legs |
Areflexia or hyporeflexia |
Features that strongly support the diagnosis |
Progressive motor weakness up to 4 wk |
Relative symmetry of symptoms |
Mild sensory involvement |
Cranial nerve involvement, especially bilateral facial |
Weakness |
Autonomic dysfunction |
Pain |
Albuminocytological dissociation in CSF |
Electrodiagnostic features of demyelination |
Features that should raise doubt about the diagnosis |
Respiratory failure with limited weakness of limbs at onset |
Severe sensory signs at onset |
Bladder or bowel dysfunction at onset and persistence of dysfunction in the disease course |
Fever at onset |
Sharp sensory level |
Slow progression with limited weakness without |
Respiratory involvement |
Persistent asymmetry of motor weakness |
Mono/polymorphonuclear leukocytosis in CSF |
- Citation: Nayak R. Practical approach to the patient with acute neuromuscular weakness. World J Clin Cases 2017; 5(7): 270-279
- URL: https://www.wjgnet.com/2307-8960/full/v5/i7/270.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v5.i7.270