Familial Mediterranean Fever (Recurrent Polyserositis) | oneAMYLOIDOSISvoice
Reference Materials

Familial Mediterranean Fever (Recurrent Polyserositis)

key information

source: Europe PMC

year: 2016

authors: Mordechai Shohat

summary/abstract:

Familial Mediterranean fever (FMF) is divided into two phenotypes: Type 1 and Type 2
 
• FMF type 1 is characterized by recurrent short episodes of inflammation and serositis including fever, peritonitis, synovitis, pleuritis, and, rarely, pericarditis and meningitis. The symptoms and severity vary among affected individuals, sometimes even among members of the same family. Amyloidosis, which can lead to renal failure, is the most severe complication, if untreated.
 
• FMF type 2 is characterized by amyloidosis as the first clinical manifestation of FMF in an otherwise asymptomatic individual.
 
organization: Sackler School of Medicine, Israel

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