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Case Report

A case of acute motor sensory axonal neuropathy presenting reversible conduction block

Dongah Lee1, Hyung Chan Kim1, Kang Min Park1, Jinse Park1, Sam Yeol Ha1, Sung Eun Kim1, Byung In Lee1, Jong Kuk Kim2, Byeola Yoon2, Kyong Jin Shin1
Annals of Clinical Neurophysiology 2018;20(1):49-52.
Published online: January 31, 2018
1Department of Neurology, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea
2Department of Neurology, Dong-A University Hospital, Dong-A University College of Medicine, Busan, Korea
Corresponding author:  Kyong Jin Shin, Tel: +82-51-797-2080, Fax: +82-51-797-1196, 
Email: neurof@naver.com
Received: 22 August 2017   • Revised: 21 December 2017   • Accepted: 28 December 2017
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Reversible conduction block (RCB) was rare in patients with acute motor sensory axonal neuropathy (AMSAN). A-46-year-old man presented with paresthesia, weakness, diplopia, and dysarthria. Nerve conduction study (NCS) exhibited axonal changes with conduction block in motor and sensory nerves. His symptoms were rapidly progressed and recovered. Conduction block was disappeared in the follow-up NCS performed after 2 weeks. The AMSAN case with RCB showed rapid progress and rapid recovery of clinical symptoms as acute motor axonal neuropathy patients with RCB.

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