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A young adult presenting with granulomatous hepatitis and nephrotic syndrome: A case report
Amyloidosis is a rare disease characterised by the deposition of insoluble extracellular fibrillar proteins in various tissues of the body. The pattern of manifestation is organ dependent and also on whether the disease is localised or systemic, primary or secondary. Primary systemic amyloidosis is...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496606/ https://www.ncbi.nlm.nih.gov/pubmed/23095309 http://dx.doi.org/10.1186/1755-7682-5-29 |