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Post-vaccine glomerulonephritis in an infant with hereditary C2 complement deficiency: case study
We describe a case of a post vaccine immune complex-mediated glomerulonephritis in an infant with compound heterozygous mutations of C2 complement component gene, which is the first such case in the literature. The three and a half months old boy presented with clinical and laboratory signs of nephr...
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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Croatian Medical Schools
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3893984/ https://ncbi.nlm.nih.gov/pubmed/24382852 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3325/cmj.2013.54.569 |
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