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dc.contributor.authorNosratinia, H
dc.date.accessioned2018-08-26T09:37:34Z
dc.date.available2018-08-26T09:37:34Z
dc.date.issued2004
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/58119
dc.description.abstractTakayasu's arteritis is a large vessel vasculitis whose histopathologic findings are indistinguishable. Takayasu's arteritis is seldom reported because of being a rare disease. The incidence of Takayasu's arteritis is 5 to 8 times higher in Japan, India, and Africa than in the United States. This disease occurs mostly in young women, preferentially affecting the aorta and its major branches, and causes stenotic and ectatic changes. The best method for its evaluation is angiography and managements are medical and surgical.
dc.language.isoEnglish
dc.relation.ispartofPakistan Journal of Medical Sciences
dc.subjectadult
dc.subjectangiography
dc.subjectaorta arch syndrome
dc.subjectarticle
dc.subjectbrain perfusion
dc.subjectcase report
dc.subjectclinical feature
dc.subjectcollateral circulation
dc.subjectfemale
dc.subjecthistopathology
dc.subjecthuman
dc.subjectpatient referral
dc.subjectphysical examination
dc.titleTakayasu's arteritis
dc.typeArticle
dc.citation.volume20
dc.citation.issue3
dc.citation.spage248
dc.citation.epage250
dc.citation.indexScopus


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