Familial Mediterranean fever and membranous glomerulonephritis: report of a case.

Abstract:

:Familial Mediterranean fever (FMF) is an autosomal recessive genetic disease characterized by recurrent attacks of fever and painful episodes of sterile polyserositis. Kidney involvement may occur as a result of secondary amyloidosis during the course of FMF. Previously, different types of glomerulopathies such as IgM and IgA nephropathy, crescentic glomerulonephritis, diffuse proliferative glomerulonephritis, minimal change disease, and membranoproliferative glomerulonephritis were rarely reported. We herein represent a first case of membranous glomerulonephritis who had complete remission with colchicine treatment in the course of familial Mediterranean fever.

journal_name

Ren Fail

journal_title

Renal failure

authors

Ceri M,Unverdi S,Altay M,Unverdi H,Ensari A,Duranay M

doi

10.3109/08860221003640090

subject

Has Abstract

pub_date

2010-01-01 00:00:00

pages

401-3

issue

3

eissn

0886-022X

issn

1525-6049

journal_volume

32

pub_type

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