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DC FieldValueLanguage
dc.contributor.author김미정-
dc.date.accessioned2019-12-04T06:53:30Z-
dc.date.available2019-12-04T06:53:30Z-
dc.date.issued2018-02-
dc.identifier.citationAnnals of Rehabilitation Medicine, v. 42, no. 1, page. 184-188en_US
dc.identifier.issn2234-0645-
dc.identifier.issn2234-0653-
dc.identifier.urihttps://www.e-arm.org/journal/view.php?doi=10.5535/arm.2018.42.1.184-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/117312-
dc.description.abstractHennekam syndrome is a rare autosomal recessive disorder resulting from malformation of the lymphatic system. The characteristic signs of Hennekam syndrome are lymphangiectasia, lymph edema, facial anomalies, and mental retardation. This is a case in which a patient presented with left-arm lymphedema, facial-feature anomalies, and multiple organ lymphangiectasia consistent with symptoms of Hennekam syndrome. There is no curative therapy at this time, but rehabilitative treatments including complete decongestive therapy for edema control appeared to be beneficial.en_US
dc.language.isoen_USen_US
dc.publisher대한재활의학회en_US
dc.subjectLymphedemaen_US
dc.subjectHennekam lymphangiectasia lymphedema syndromeen_US
dc.titleHennekam syndrome: A case reporten_US
dc.typeArticleen_US
dc.relation.no1-
dc.relation.volume42-
dc.identifier.doi10.5535/arm.2018.42.1.184-
dc.relation.page184-188-
dc.relation.journalAnnals of Rehabilitation Medicine-
dc.contributor.googleauthor이영국-
dc.contributor.googleauthor김승찬-
dc.contributor.googleauthor박시복-
dc.contributor.googleauthor김미정-
dc.contributor.googleauthorLee, Yeong Guk-
dc.contributor.googleauthorKim, Seung Chan-
dc.contributor.googleauthorPark, Si-Bog-
dc.contributor.googleauthorKim, Mi Jung-
dc.relation.code2018021697-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidkimmjreh-


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