Familial Mediterranean fever is a hereditary disorder that affects people of Mediterranean countries regions. this disorder tends to affect Greeks, Armenians, Sephardim, Turks and people of Arab descent. familial mediterranean fever attack is believed to be caused by mutations in the gene mefv.
treatment is required to prevent further attacks. those who do not seek treatment for familial Mediterranean fever will often experience a large amount of protein buildup, which can lead to kidney failure. Treatment for this disorder include non-steroidal anti-inflammatory drugs like colchicine therapy, often through intravenous drip.
Familial Mediterranean fever is also known as periodic disease, recurrent polyserositis, FMF, and periodic peritonitis. This disease is relatively rare, but it is a serious condition that can be corrected immediately often, mediterranean fever misdiagnosed because the symptoms of this disease can mimic appendicitis
diagnosis. mediterranean fever is often concluded based on family history, an elevated white blood cells, and repeat symptoms. in addition, a genetic test is given to individual patients. while Mediterranean fever is probably associated with a mefv gene mutation, are the reasons why this mutation leads to Mediterranean fever attacks largely unknown.
on the discrepancy between the pain of each individual, and the reasons why inflammation occurs within particular parts of the body not clear at this time.