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 Failjournal_title
Renal failureauthors
Ceri M,Unverdi S,Altay M,Unverdi H,Ensari A,Duranay Mdoi
10.3109/08860221003640090subject
Has Abstractpub_date
2010-01-01 00:00:00pages
401-3issue
3eissn
0886-022Xissn
1525-6049journal_volume
32pub_type
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