Journals / Göztepe Tıp Dergisi / 2003 / Cilt: 18 - Sayı: 4

Familial Mediterranian fever

22 aylık bir erkek hastada ailesel Akdeniz ateşi artriti

Pages
251–252
Publication Date
2022-10-17
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Here we report a case diagnosed as FMF by clinical progress and family history and supported by genetic diagnosis.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Familial mediterranian fever (FMF) is a genetic disease characterized by recurrent febrile attacks and inflammation of serous membranes.
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Key Findings & Data:Artralgia and artritis can be seen in 75 % of patints.
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Conclusion & Impact:Here we report a case diagnosed as FMF by clinical progress and family history and supported by genetic diagnosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Familial mediterranian fever (FMF) is a genetic disease characterized by recurrent febrile attacks and inflammation of serous membranes. Artralgia and artritis can be seen in 75 % of patints. Here we report a case diagnosed as FMF by clinical progress and family history and supported by genetic diagnosis.

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Cite This Article

BİLGİÇ, E., YILMAZ, Ç., HATİPOĞLU, H., PİNÇE, O., ŞİRANECİ, R., KASAPÇOPUR, Ö., TÜREL, Ö., KALE, S. (2022). Familial Mediterranian fever. Göztepe Tıp Dergisi, Cilt: 18 - Sayı: 4, 251–252. https://ajindex.com/articles/526520

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References (6)

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  4. Majeed HA, Rawashdeh M: The clinical patterns of arthritis in children with FMF. QJ Med 90:37-43, 1997
  5. Özen S, Kraaslan Y, Özdemir O: Prevalence of JCA and FMF in Turkey: A field study. The Journal of Rheumatology 25:12, 1998
  6. Saatçi U, Özen S, Özdemir S, et al: FMF in children: report of a large series and discussion of the risk and prognostic factors of amyloidosis.