| Literature DB >> 15481855 |
L Koukoui1, A Blau, J Kopolovic, M Pras, A Livneh.
Abstract
IgA nephropathy is the most common primary glomerulopathy. Currently, no satisfactory treatment is available and as a result, a significant proportion of affected patients progress to end-stage renal disease. We present a patient with IgA nephropathy in whom continuous colchicine treatment induced remission, which has lasted for 22 years. The patient was a carrier of a mutation in the FMF gene (MEFV). This case raises hopes for a better prognosis in at least one subgroup of IgA nephropathy, consisting of patients who happen to be heterozygous carriers of MEFV mutations.Entities:
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Year: 2004 PMID: 15481855 DOI: 10.5414/cnp62226
Source DB: PubMed Journal: Clin Nephrol ISSN: 0301-0430 Impact factor: 0.975