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dc.contributor.author권석경-
dc.contributor.author이상래-
dc.contributor.author박종완-
dc.contributor.author최종환-
dc.contributor.author김진석-
dc.contributor.author박상원-
dc.date.accessioned2017-08-08T09:06:38Z-
dc.date.available2017-08-08T09:06:38Z-
dc.date.issued2015-
dc.identifier.citationKeimyung Medical Journal, Vol.45(2) : 216-219, 2015-
dc.identifier.otherKMJ-2015-038-
dc.identifier.urihttp://kumel.medlib.dsmc.or.kr/handle/2015.oak/15689-
dc.description.abstractThe hypoglossal nerve palsy receives only brief mention in most textbooks and compared with other cranial nerve palsies, 12th nerve palsy is much less common. A literature review revealed that in most cases, isolated hypoglossal nerve palsy indicates the presence of an intracranial or extracranial space occupying lesion, head and neck injury, vascular abnormality, infection, autoimmune disease or neuropathy. Reports of idiopathic cases are rare and treated with steroid therapy. We report a 38-year-old woman with isolated hypoglossal nerve palsy improved spontaneously without steroid use. Considering our experience with isolated hypoglossal nerve palsy, we believe that no therapy is required in the patients with hypoglossal nerve palsy of probably idiopathic causes.-
dc.description.statementofresponsibilityopen-
dc.publisherKeimyung University School of Medicine-
dc.rightsBY_NC_ND-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kr-
dc.subjectHypoglossal nerve palsy-
dc.subjectIdiopathic-
dc.subjectSteroid-
dc.title스테로이드 사용 없이 호전된 특발성 단독설하신경마비 1례-
dc.title.alternative(A)case of improved idiopathic isolated hypoglossal nerve palsy without use of steroid-
dc.typeArticle-
dc.contributor.alternativeauthorSeok Kyung Kwon-
dc.contributor.alternativeauthorSang Lae Lee-
dc.contributor.alternativeauthorJong Wan Park-
dc.contributor.alternativeauthorJong Whan Choi-
dc.contributor.alternativeauthorJin Suk Kim-
dc.contributor.alternativeauthorSang Won Park-
dc.citation.volume45-
dc.citation.number2-
dc.citation.startpage216-
dc.citation.titleKeimyung Medical Journal-
dc.citation.endpage219-


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