The recurrent inflammatory attacks in FMF cause intense acute symptoms and confer a markedly increased relative risk of developing AA amyloidosis and eventually end-stage renal disease. Prior to the colchicine era, this was a major scourge particularly around the Eastern Mediterranean. Other potential complications of FMF include destructive arthritis, adhesions, subfertility, and vasculitis. Fortunately, these remain very rare, and with long-term treatment, recent studies suggest that both complications and mortality for FMF appear very close to age-matched healthy controls.
CITATION STYLE
Lachmann, H. J. (2015). Long-Term Complications of Familial Mediterranean Fever. In Rare Diseases of the Immune System (Vol. 3, pp. 91–105). Springer Nature. https://doi.org/10.1007/978-3-319-14615-7_6
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