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Information Journal Paper

Title

CASE REPORT OF FAMILIAN MEDITRANIAN FEVER (FMF)

Pages

  15-17

Abstract

FAMILIAN MEDITRANIAN FEVER (FMF) is an inherited disorder and characterized by recurrent self limiting attracts of fever and polyserositis.Because of rarity of this disease and the difficulty of diagnosis, the physician's presence of mind is a necessary thing. The patient is a 16 years old boy who had recurrent attacks of abdominal pain, headache, fever, rash and arthritis. The interval of his attacks was variable between 1-2 years and 2 times in a week. He had an appendectomy about 8 years ago.Because of arthritis, with probable diagnosis of R.F., he recieved penicillin monthly.During the attacks, lab tests showed, leukocytosis elevated sedimentation rate and positive CRP.The CT of abdomen and transient of small bowell were normal.The use of COLCHICINE 0.5mg two times in a day caused arrest of attacks.This case is reported because of its rarity and for physicians' presence of mind.

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  • Cite

    APA: Copy

    SOUFIAN, MASOUMEH. (2001). CASE REPORT OF FAMILIAN MEDITRANIAN FEVER (FMF). ARAK MEDICAL UNIVERSITY JOURNAL (AMUJ), 3(4 (13)), 15-17. SID. https://sid.ir/paper/69265/en

    Vancouver: Copy

    SOUFIAN MASOUMEH. CASE REPORT OF FAMILIAN MEDITRANIAN FEVER (FMF). ARAK MEDICAL UNIVERSITY JOURNAL (AMUJ)[Internet]. 2001;3(4 (13)):15-17. Available from: https://sid.ir/paper/69265/en

    IEEE: Copy

    MASOUMEH SOUFIAN, “CASE REPORT OF FAMILIAN MEDITRANIAN FEVER (FMF),” ARAK MEDICAL UNIVERSITY JOURNAL (AMUJ), vol. 3, no. 4 (13), pp. 15–17, 2001, [Online]. Available: https://sid.ir/paper/69265/en

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