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Article

Extensive thrombosis in a patient with familial Mediterranean fever, despite hyperimmunoglobulin D state in serum. [corrected].

Journal of Korean medical science - 1 Feb 2013

Joo Kowoon, Park Won, Chung Moon-Hyun, Lim Mie-Jin, Jung Kyong Hee, Heo Yoonseok, Kwon Seong-Ryul

Abstract excerpt

Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent episodes of fever accompanied by peritonitis, pleuritis, arthritis, or erysipelas-like erythema. It is known to occur mainly among Mediterranean and Middle Eastern populations such as non-Ashkenazi Jews, Arabs, Turks, and Armenians. FMF is not familiar to clinicians beyond this area and diagnosing FMF can be...

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Source

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Identifiers

PMID: 23400211
DOI: 10.3346/jkms.2013.28.2.328
PMCID: PMC3565148

Genes

MEFV

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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