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Amyloid nephropathy

Amyloidosis is an uncommon disease that is characterized by abnormal extracellular deposition of misfolded protein fibrils leading to organ dysfunction. The deposited proteins display common chemical and histologic properties but can vary dramatically in their origin. Kidney disease is a common mani...

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Detalles Bibliográficos
Autores principales: Khalighi, Mazdak A., Dean Wallace, W., Palma-Diaz, Miguel F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377792/
https://www.ncbi.nlm.nih.gov/pubmed/25852856
http://dx.doi.org/10.1093/ckj/sfu021
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author Khalighi, Mazdak A.
Dean Wallace, W.
Palma-Diaz, Miguel F.
author_facet Khalighi, Mazdak A.
Dean Wallace, W.
Palma-Diaz, Miguel F.
author_sort Khalighi, Mazdak A.
collection PubMed
description Amyloidosis is an uncommon disease that is characterized by abnormal extracellular deposition of misfolded protein fibrils leading to organ dysfunction. The deposited proteins display common chemical and histologic properties but can vary dramatically in their origin. Kidney disease is a common manifestation in patients with systemic amyloidosis with a number of amyloidogenic proteins discovered in kidney biopsy specimens. The emergence of mass spectrometry-based proteomics has added to the diagnostic accuracy and overall understanding of amyloidosis. This in-depth review discusses the general histopathologic features of renal amyloidosis and includes an in-depth discussion of specific forms of amyloid affecting the kidney.
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spelling pubmed-43777922015-04-07 Amyloid nephropathy Khalighi, Mazdak A. Dean Wallace, W. Palma-Diaz, Miguel F. Clin Kidney J Original Contributions Amyloidosis is an uncommon disease that is characterized by abnormal extracellular deposition of misfolded protein fibrils leading to organ dysfunction. The deposited proteins display common chemical and histologic properties but can vary dramatically in their origin. Kidney disease is a common manifestation in patients with systemic amyloidosis with a number of amyloidogenic proteins discovered in kidney biopsy specimens. The emergence of mass spectrometry-based proteomics has added to the diagnostic accuracy and overall understanding of amyloidosis. This in-depth review discusses the general histopathologic features of renal amyloidosis and includes an in-depth discussion of specific forms of amyloid affecting the kidney. Oxford University Press 2014-04 2014-03-13 /pmc/articles/PMC4377792/ /pubmed/25852856 http://dx.doi.org/10.1093/ckj/sfu021 Text en © The Author 2014. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For permissions, please email: journals.permissions@oup.com. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Contributions
Khalighi, Mazdak A.
Dean Wallace, W.
Palma-Diaz, Miguel F.
Amyloid nephropathy
title Amyloid nephropathy
title_full Amyloid nephropathy
title_fullStr Amyloid nephropathy
title_full_unstemmed Amyloid nephropathy
title_short Amyloid nephropathy
title_sort amyloid nephropathy
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377792/
https://www.ncbi.nlm.nih.gov/pubmed/25852856
http://dx.doi.org/10.1093/ckj/sfu021
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