Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII

Amyloidosis is characterized by extracellular deposition of misfolded proteins as insoluble fibrils. Most renal amyloidosis cases are Ig light chain, AA, or leukocyte chemotactic factor 2 amyloidosis, but rare hereditary forms can also involve the kidneys. Here, we describe the case of a 61-year-old...

詳細記述

保存先:
書誌詳細
出版年:J Am Soc Nephrol
主要な著者: Nasr, Samih H., Dasari, Surendra, Hasadsri, Linda, Theis, Jason D., Vrana, Julie A., Gertz, Morie A., Muppa, Prasuna, Zimmermann, Michael T., Grogg, Karen L., Dispenzieri, Angela, Sethi, Sanjeev, Highsmith, W. Edward, Merlini, Giampaolo, Leung, Nelson, Kurtin, Paul J.
フォーマット: Artigo
言語:Inglês
出版事項: American Society of Nephrology 2017
主題:
Brief Communications
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5280007/
https://ncbi.nlm.nih.gov/pubmed/27297947
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2015111228
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