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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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Publicat a:Clin Nephrol Case Stud
Autors principals: Pleyer, Christopher, Flesche, Jan, Saeed, Fahad
Format: Artigo
Idioma:Inglês
Publicat: Dustri-Verlag Dr. Karl Feistle 2015
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Accés en línia: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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