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Miller Fisher syndrome mimicking Wernicke encephalopathy during pregnancy
서정화,Mi-Ri Kang,Byeola Yoon,Ki-Hwan Ji,오성일 대한임상신경생리학회 2019 Annals of Clinical Neurophysiology Vol.21 No.1
Miller Fisher syndrome (MFS) is characterized by ataxia, areflexia, and ophthalmoparesis. Here we present a case of MFS mimicking Wernicke encephalopathy (WE) during pregnancy. A 31-year-old woman at 8 weeks of gestation presented with diplopia and ataxia after experiencing nausea and vomiting for several weeks. We initiated thiamine based on a suspicion of WE, which produced no clear effects. However, her symptoms began to improve following intravenous immunoglobulin treatment, and other findings finally lead to a diagnosis of MFS. Because ataxia and ophthalmoparesis can be misdiagnosed as WE during pregnancy, clinicians should consider MFS in the differential diagnosis.
A case of acute motor sensory axonal neuropathy presenting reversible conduction block
Dongah Lee,Hyung Chan Kim,Kang Min Park,Jinse Park,Sam Yeol Ha,Sung Eun Kim,Byung In Lee,김종국,Byeola Yoon,Kyong Jin Shin 대한임상신경생리학회 2018 Annals of Clinical Neurophysiology Vol.20 No.1
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.
A case of acute motor sensory axonal neuropathy presenting reversible conduction block
Lee, Dongah,Kim, Hyung Chan,Park, Kang Min,Park, Jinse,Ha, Sam Yeol,Kim, Sung Eun,Lee, Byung In,Kim, Jong Kuk,Yoon, Byeola,Shin, Kyong Jin The Korean Society of Clinical Neurophysiology 2018 Annals of Clinical Neurophysiology Vol.20 No.1
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.