Karyomegalic interstitial nephritis with a novel FAN1 gene mutation and concurrent ALECT2 amyloidosis

Karyomegalic interstitial nephritis with a novel FAN1 gene mutation and concurrent ALECT2 amyloidosis

Abstract Background Karyomegalic interstitial nephritis (KIN) is a rare hereditary cause of chronic kidney disease. It typically causes progressive renal impairment with haemoproteinuria requiring renal replacement therapy before 50 years of age. It has been associated with mutations in the Fanconi...

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Bibliographic Details
Main Authors: Steven Law, Julian Gillmore, Janet A. Gilbertson, Paul Bass, Alan D. Salama
Format: Article
Language:English
Published: BMC 2020-02-01
Series:BMC Nephrology
Subjects:
Karyomegalic interstitial nephritis
Interstitial nephritis
Leukocyte chemotactic factor 2 amyloidosis
ALECT2
Amyloidosis
Chronic kidney disease
Online Access:http://link.springer.com/article/10.1186/s12882-020-01733-9

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http://link.springer.com/article/10.1186/s12882-020-01733-9

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