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A Rare Presentation of Familial Mediterranean fever; Acute Scrotum and Hydrocele Amyloidosis

BACKGROUND: Familial Mediterranean Fever (FMF) is a genetic disease characterized by recurrent febrile attacks and inflammation of serous membranes. Amyloidosis is frequent in untreated FMF patients and is also the most important complication of FMF. It is generally seen with renal, hepatic, gastroi...

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Bibliografiset tiedot
Päätekijät: Yilmaz, Resul, Ozer, Samet
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Tehran University of Medical Sciences 2010
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3446044/
https://ncbi.nlm.nih.gov/pubmed/23056732
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