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IgG4-Related Kidney Disease: A Curious Case of Interstitial Nephritis with Hypocomplementemia
IgG4-related kidney disease has been relatively newly recognized over the last two decades as a combination of an autoimmune and allergic disorder, with elevated serum IgG4 level and hypocomplementemia among its characteristic features. Here we report the case of a man with interstitial nephritis pr...
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| Pubblicato in: | Case Rep Nephrol Dial |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
S. Karger AG
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6547283/ https://ncbi.nlm.nih.gov/pubmed/31192228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000500296 |
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