Takayasu Arteritis

dc.contributor.authorGökçe, Şule
dc.contributor.authorGüneş, Deniz
dc.contributor.authorAltunordu, Gizem
dc.contributor.authorAmanova, Günay
dc.contributor.authorAkşit, Sadık
dc.date.accessioned2020-12-01T12:33:15Z
dc.date.available2020-12-01T12:33:15Z
dc.date.issued2018
dc.departmentEge Üniversitesien_US
dc.description.abstractTakayasu arteritis is a rare systemic vasculitis. It is seen in young female adolescents as two-four times more than males. the etiology of this vasculitis also called "Japanese Disease" due to its high incidence in Japan, has not yet been clarified. Patients might present with non-specific findings in the early phase of the disease. in this article we present a case of a 16-year-old girl who has been referred to our clinic for weakness and fatigue. She had been diagnosed with iron deficiency many times in other centers. However, she applied to our clinic because her complaints did not decrease. the patient was diagnosed with Takayasu arteritis with the history and clinical findings. in this article we aimed to call attention to the Takayasu arteritis and to emphasise once again the importance of detailed history and physical examination.en_US
dc.identifier.doi10.5336/caserep.2017-58225
dc.identifier.endpage116en_US
dc.identifier.issn2147-9291
dc.identifier.issn2147-9291
dc.identifier.issue3en_US
dc.identifier.startpage113en_US
dc.identifier.urihttps://doi.org/10.5336/caserep.2017-58225
dc.identifier.urihttps://app.trdizin.gov.tr//makale/TXpVMk56VXlNZz09
dc.identifier.urihttps://hdl.handle.net/11454/66505
dc.identifier.volume26en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofTürkiye Klinikleri Journal of Case Reportsen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject0-Belirleneceken_US
dc.titleTakayasu Arteritisen_US
dc.typeArticleen_US

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