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Article

Mesangial proliferative glomerulonephritis in familial Mediterranean fever patient with E148Q mutation: the first case report.

International urology and nephrology - 1 Apr 2013

Eroglu Eray, Kocyigit Ismail, Ates Ozturk, Unal Aydin, Sipahioglu Murat Hayri, Akgun Hulya, Tokgoz Bulent, Oymak Oktay

Abstract excerpt

Familial Mediterranean fever (FMF) is an autosomal recessive hereditary disease characterized by recurrent attacks of fever, usually accompanied by sterile polyserositis. Although amyloidosis is the most common renal involvement, non-amyloid renal lesions, such as glomerulonephritis, have been described in patients with FMF. In this report, we present the first case of an FMF patient with heterozygous mutation of...

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PMID: 22261745
DOI: 10.1007/s11255-012-0124-1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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