Corrigendum to “Multiple cranial neuropathy (a teaching case)” MSARD 2(4) (2013) 395–398

dc.contributor.authorToro, Jaime
dc.contributor.authorMillán, Carlos
dc.contributor.authorDíaz, Camilo
dc.contributor.authorReyes, Saúl
dc.contributor.orcidToro, Jaime [0000-0001-7129-0058]
dc.date.accessioned2020-07-06T16:26:19Z
dc.date.available2020-07-06T16:26:19Z
dc.date.issued2014
dc.description.abstractenglishThere are few reports of the multiple cranial neuropathy variant of Guillain-Barré Syndrome (GBS). Patients usually present with facial diplegia, lower cranial nerve involvement and hypo or areflexia. It is crucial to identify promptly this unusual cranial variant but the clinical characteristics remain poorly defined. This GBS variant usually has a rapid progressive course with respiratory muscle paralysis. Most of the patients recover well, although the process is slow. We report a 54 year old man presenting with facial diplegia, progressive ophthalmoplegia, lower cranial nerve involvement, sensory ataxia and generalized areflexia. This GBS variant is very unusual and seldom described in the literature; it is oftenly misdiagnosed. The clinical features and nerve conduction studies (absent F-waves, motor conduction block) provide evidence to support a diagnosis of an acute demyelinating polyneuropathy consistent with a regional cranial variant of GBS. & 2013 Elsevier B.V. All rights reserved.eng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.1016/j.msard.2013.12.005
dc.identifier.instnameinstname:Universidad El Bosquespa
dc.identifier.issn2211-0348
dc.identifier.reponamereponame:Repositorio Institucional Universidad El Bosquespa
dc.identifier.repourlhttps://repositorio.unbosque.edu.co
dc.identifier.urihttps://hdl.handle.net/20.500.12495/3323
dc.language.isoeng
dc.publisherMultiple Sclerosis and Related Disordersspa
dc.publisher.journalMultiple Sclerosis and Related Disordersspa
dc.relation.ispartofseriesMultiple Sclerosis and Related Disorders, 2211-0348, Vol. 3, Nro 3, 2014, p. 416spa
dc.relation.urihttps://www.sciencedirect.com/science/article/pii/S2211034813001375
dc.rights.accessrightshttps://purl.org/coar/access_right/c_abf2
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.rights.accessrightsAcceso abierto
dc.rights.creativecommons2014
dc.rights.localAcceso abiertospa
dc.subject.decsSíndrome de Guillain-Barréspa
dc.subject.decsArreflexia vestibularspa
dc.subject.decsImunoglobulinaspa
dc.subject.keywordsGuillain-Barré syndrome variantspa
dc.subject.keywordsMultiple cranial neuropathyspa
dc.subject.keywordsPolyneuritis cranialisspa
dc.subject.keywordsAreflexiaspa
dc.subject.keywordsIntravenous immunoglobulinspa
dc.titleCorrigendum to “Multiple cranial neuropathy (a teaching case)” MSARD 2(4) (2013) 395–398spa
dc.type.coarhttps://purl.org/coar/resource_type/c_6501
dc.type.driverinfo:eu-repo/semantics/article
dc.type.hasversioninfo:eu-repo/semantics/publishedVersion
dc.type.localArtículo de revista

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