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dc.contributor.authorOtieno, FO
dc.contributor.authorOyoo, GO
dc.contributor.authorOtieno, CF
dc.contributor.authorOmondi, EA
dc.date.accessioned2015-06-10T05:20:01Z
dc.date.available2015-06-10T05:20:01Z
dc.date.issued2015
dc.identifier.citationAfrican Journal of Rheumatology Vol 3, No 1 (2015)en_US
dc.identifier.urihttp://www.ajol.info/index.php/ajr/article/view/117498
dc.identifier.urihttp://hdl.handle.net/11295/84484
dc.description.abstractIntroduction: Adult Still’s Disease (ASD) is a systemic inflammatory disorder of unknown etiology, typically characterized by a clinical triad (daily spiking high fevers, evanescent rash, arthritis), and a biological triad (hyperferritinemia, hyperleukocytosis with neutrophilia and abnormal liver function test). Objective: This case series set out to describe the clinical characteristics of patients with ASD seen at a rheumatology clinic in Nairobi. Results: After a record search, 8 patients were noted to have ASD. Fever and arthritis were noted to be most predominant presenting features with almost all the patients having hyperferritinemia.en_US
dc.language.isoenen_US
dc.titleClinical presentation of patients with adult onset still’s disease in Nairobi: case seriesen_US
dc.typeArticleen_US
dc.type.materialenen_US


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