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An unusual manifestation in a patient with adult-onset Still’s disease: Minimal glomerular lesion
Adult-onset Still’s disease (AOSD) is a multisystem inflammatory disease of unknown etiology. It is characterized by arthritis, hectic fever, transient rash and visceral lesions such as pleuropericarditis, lymphadenopathy and hepato splenomegaly. Although kidney involvement may appear in some cases...
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| Vydáno v: | Eur J Rheumatol |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medical Research and Education Association
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5042222/ https://ncbi.nlm.nih.gov/pubmed/27708893 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/eurjrheumatol.2014.027 |
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