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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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Pubblicato in:Clin Nephrol Case Stud
Autori principali: Pleyer, Christopher, Flesche, Jan, Saeed, Fahad
Natura: Artigo
Lingua:Inglês
Pubblicazione: Dustri-Verlag Dr. Karl Feistle 2015
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Accesso online: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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