Key result
A trial of therapy resulted in the cessation of symptoms in two cases of familial Mediterranean fever.
Case Report (n=2)
Prompt evaluation and treatment of familial Mediterranean fever can improve quality of life and prevent complications such as amyloidosis.
Prompt evaluation of recurrent fevers in children may identify FMF and preserve quality of life; leaves open standardized criteria for atypical presentations.
Familial Mediterranean fever, an autosomal recessive disorder, is a member of the periodic fever syndromes, and considered to be the most common cause of recurrent febrile episodes in children. It is important to understand the disorder as familial Mediterranean fever falls on a spectrum of various presentations; the recurrent episodes of familial Mediterranean fever may be so severe that the quality of life may be affected in such patients. Therefore, physicians should not delay the evaluation in such cases and promptly initiate treatment to not only improve quality of life but to also avoid complications, such as amyloidosis. This study reports two different cases of familial Mediterranean fever, with varying clinical presentations, and established diagnosis via genetic testing as well as cessation of symptoms with a trial of therapy. Furthermore, this study discusses the various manifestations of familial Mediterranean fever, laboratory findings, and current therapies available for management.
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Khan et al. (2017) conducted a case report in Familial Mediterranean fever (n=2). Therapy was evaluated on Cessation of symptoms. A trial of therapy resulted in the cessation of symptoms in two cases of familial Mediterranean fever.
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