Amyloidosis in familial Mediterranean fever patients: correlation with MEFV genotype and SAA1 and MICA polymorphisms effects

BACKGROUND: Familial mediterranean fever (FMF) is a recessively inherited disease characterized by recurrent crises of fever, abdominal, articular and/or thoracic pain. The most severe complication is the development of renal amyloidosis. Over 35 mutations have been discovered so far in the gene res...

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Hlavní autoři: Medlej-Hashim, Myrna, Delague, Valérie, Chouery, Eliane, Salem, Nabiha, Rawashdeh, Mohammed, Lefranc, Gérard, Loiselet, Jacques, Mégarbané, André
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2004
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC356915/
https://ncbi.nlm.nih.gov/pubmed/15018633
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-5-4
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