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...

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Bibliographic Details
Published in:J Am Soc Nephrol
Main Authors: 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.
Format: Artigo
Language:Inglês
Published: American Society of Nephrology 2017
Subjects:
Brief Communications
Online Access: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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