Published online Jul 16, 2017. doi: 10.12998/wjcc.v5.i7.270
Peer-review started: February 12, 2017
First decision: March 7, 2017
Revised: April 20, 2017
Accepted: May 12, 2017
Article in press: May 15, 2017
Published online: July 16, 2017
Processing time: 165 Days and 22.1 Hours
Core tip: Acute neuromuscular paralysis is a clinical syndrome characterized by rapid onset muscle weakness progressing to maximum severity within several days to weeks. It is a neurological emergency which requires immediate and careful investigations to determine the etiology because accurate diagnosis has significant impact on therapy and prognosis. Disorder is classified based on the site of defect in motor unit pathway, i.e., anterior horn cells, nerve root, peripheral nerve, neuromuscular junction or muscle. Identification of the cause is primarily based on a good medical history and detailed clinical examination supplemented with neurophysiologic investigations and sometimes few specific laboratory tests. Medical history and neurological examination should be focused on the onset, progression, pattern and severity of muscle weakness as well as cranial nerves testing and tests for autonomic dysfunction.