familial Mediterranean fever otherwise known as periodic disease, has a genomic etiology, diagnosed in 6% of Europeans, but more common in the descendants of the ancient peoples of the Mediterranean.
Symptomatic familial Mediterranean fever manifests itself in the system crashes. Form of the disease may be vascular, meningeal, pleural, joint and combined. A key complication of the pathology of acute peritonitis. In the absence of treatment of periodic disease leads to amyloidosis, renal failure and death.
the Debut of a periodic disease at the age of 20-25 years, after which the patient is assigned to a lifelong drug therapy protivopodagricakih funds.
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