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dc.contributor.authorBarzegar, M
dc.contributor.authorRouhi, AHJ
dc.contributor.authorFarhoudi, M
dc.contributor.authorSardashti, S
dc.date.accessioned2018-08-26T08:04:31Z
dc.date.available2018-08-26T08:04:31Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/49585
dc.description.abstractAlthough it is a sporadic disease, few studies have reported cases of Guillain Barre Syndrome (GBS) in families which postulate a genetic susceptibility. Human leukocyte antigen (HLA) typing is an area of discussion in GBS though none of them are considered definitive. In recent years, more studies have evaluated HLA typing in sporadic cases while rarely it has been assessed in familial ones. We report a woman and her daughter experiencing GBS and their HLA typing in a 2-year interval.
dc.language.isoEnglish
dc.relation.ispartofANNALS OF INDIAN ACADEMY OF NEUROLOGY
dc.subjectFamilial
dc.subjectGuillain Barre syndrome
dc.subjecthuman leukocyte antigen typing
dc.titleA report of a probable case of familial Guillain Barre syndrome
dc.typeArticle
dc.citation.volume15
dc.citation.issue4
dc.citation.spage299
dc.citation.epage302
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.4103/0972-2327.104341


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