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Lysozyme amyloidosis – a case report and review of the literature
Lysozyme amyloidosis is an exceedingly rare hereditary autosomal dominant amyloidosis, which is characterized by the precipitation of lysozyme protein within the body, leading to multi-organ dysfunction. Herein, we present the case of a U.S. family affected by lysozyme amyloidosis. In particular, we...
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| Publicado no: | Clin Nephrol Case Stud |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dustri-Verlag Dr. Karl Feistle
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5437999/ https://ncbi.nlm.nih.gov/pubmed/29043133 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5414/CNCS108538 |
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