An Atypical Phenotype of Chronic Inflammatory Demyelinating Polyradiculoneuropathy Associated with Ocular Palsy, IgM-anti Ganglioside Antibody, and Fever-induced Recurrence
Author:
Affiliation:
1. Division of Neurology, Anti-aging, and Vascular Medicine. Department of Internal Medicine, National Defense Medical College, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/advpub/0/advpub_7526-21/_pdf
Reference10 articles.
1. 1. Kuwabara S, Isose S, Mori M, et al. Different electrophysiological profiles and treatment response in 'typical' and 'atypical' chronic inflammatory demyelinating polyneuropathy. Journal of neurology, neurosurgery, and psychiatry 86: 1054-1059, 2015.
2. 2. Martinez-Thompson JM, Snyder MR, Ettore M, et al. Composite ganglioside autoantibodies and immune treatment response in MMN and MADSAM. Muscle & nerve 57: 1000-1005, 2018.
3. 3. Likosky DJ, Kraus EE, Yuen EC. Recurrent multifocal demyelinating neuropathy with febrile illness and IgG subset deficiency. Neurology 52: 1902-1905, 1999.
4. 4. Mazzucco S, Ferrari S, Mezzina C, Tomelleri G, Bertolasi L, Rizzuto N. Hyperpyrexia-triggered relapses in an unusual case of ataxic chronic inflammatory demyelinating polyradiculoneuropathy. Neurological sciences: official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 27: 176-179, 2006.
5. 5. Ueda J, Yoshimura H, Kohara N. Pyrexia-associated relapse in chronic inflammatory demyelinating polyradiculoneuropathy. Internal medicine 57: 2723-2726, 2018.
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