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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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| Publicado no: | Eur J Rheumatol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medical Research and Education Association
2014
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| Assuntos: | |
| Acesso em linha: | 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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