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dc.contributor.authorTürker H.
dc.contributor.authorBayrak O.
dc.contributor.authorGüngör L.
dc.contributor.authorSarica M.
dc.contributor.authorOnar M.
dc.date.accessioned2020-06-21T09:20:50Z
dc.date.available2020-06-21T09:20:50Z
dc.date.issued2006
dc.identifier.issn1019-1941
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3376
dc.description.abstractMultifocal motor neuropathy is characterized by progressive, asymmetric weakness of the limbs with persistent conduction blocks (CB). Sensory loss is very rare and it also rarely presents with cranial nerve involvement and hyperreflexia. Here we described a 32-year-old woman with progressive weakness of hand muscles associated with weakness of orbicularis oculi muscles and fasciculations of tongue. The electrophysiological examination revealed persistent conduction blocks in both of the ulnar, right median and left posterior tibial nerves together with F-waves with abnormal persistence. These findings and the persistency of conduction blocks along with a response to IVIG made it likely that the diagnosis was multifocal motor neuropathy. The case seemed to be worth reporting because of her unusual clinical findings.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCranial nerve involvementen_US
dc.subjectHyperreflexiaen_US
dc.subjectMultifocal motor neuropathyen_US
dc.titleAn unusual case of multifocal motor neuropathy with cranial nerve involvement and hyperreflexiaen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume19en_US
dc.identifier.issue3en_US
dc.identifier.startpage139en_US
dc.identifier.endpage144en_US
dc.relation.journalMarmara Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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