familial Mediterranean fever

出典: meddic

再発性多発漿膜炎 recurrent polyserositis RP = 家族性地中海熱, FMF

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/04/02 03:02:28」(JST)

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  • Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry.
  • Levy R1, Gérard L2, Kuemmerle-Deschner J3, Lachmann HJ4, Koné-Paut I5, Cantarini L6, Woo P7, Naselli A8, Bader-Meunier B1, Insalaco A9, Al-Mayouf SM10, Ozen S11, Hofer M12, Frenkel J13, Modesto C14, Nikishina I15, Schwarz T16, Martino S17, Meini A18, Quartier P1, Martini A19, Ruperto N8, Neven B1, Gattorno M8; for PRINTO and Eurofever.
  • Annals of the rheumatic diseases.Ann Rheum Dis.2015 Nov;74(11):2043-9. doi: 10.1136/annrheumdis-2013-204991. Epub 2014 Jul 18.
  • OBJECTIVE: To evaluate genetic, demographic and clinical features in patients with cryopyrin-associated periodic syndrome (CAPS) from the Eurofever Registry, with a focus on genotype-phenotype correlations and predictive disease severity markers.METHODS: A web-based registry retrospectively collecte
  • PMID 25038238
  • Colchicine-clarithromycin-induced rhabdomyolysis in Familial Mediterranean Fever patients under treatment for Helicobacter pylori.
  • Cohen O1, Locketz G2, Hershko AY3,4, Gorshtein A5, Levy Y6,7,8.
  • Rheumatology international.Rheumatol Int.2015 Nov;35(11):1937-41. doi: 10.1007/s00296-015-3325-y. Epub 2015 Jul 26.
  • Chronic administration of colchicine remains a mainstay of therapy for patients with Familial Mediterranean Fever (FMF). As this medication is a strong CYP3A4 inhibitor, it has the potential to interact with many routinely used medications. One such medication is clarithromycin, itself a strong inhi
  • PMID 26210999
  • Comment on: Dysregulated mature IL-1β production in familial Mediterranean fever.
  • Dogan T1, Agilli M2.
  • Rheumatology (Oxford, England).Rheumatology (Oxford).2015 Nov;54(11):2118. doi: 10.1093/rheumatology/kev235. Epub 2015 Sep 5.
  • PMID 26342224


  • The Contribution of SAA1 Polymorphisms to Familial Mediterranean Fever Susceptibility in the Japanese Population
  • Migita Kiyoshi,Agematsu Kazunaga,Masumoto Junya,Ida Hiroaki,Honda Seiyo,Jiuchi Yuka,Izumi Yasumori,Maeda Yumi,Uehara Ritei,Nakamura Yoshikazu,Koga Tomohiro,Kawakami Atsushi,Nakashima Munetoshi,Fujieda Yuichiro,Nonaka Fumiaki,Eguchi Katsumi,Furukawa Hiroshi,Nakamura Tadashi,Nakamura Minoru,Yasunami Michio
  • PLoS ONE 8(2), e55227, 2013-02-20
  • … Background/Aims: Familial Mediterranean Fever (FMF) has traditionally been considered to be an autosomal-recessive disease, however, it has been observed that substantial numbers of patients with FMF possess only 1 demonstrable MEFV mutation. … The clinical profile of familial Mediterranean fever (FMF) may be influenced by MEFV allelic heterogeneity and other genetic and/or environmental factors. …
  • NAID 120005230926
  • Mediterranean mimicker
  • Arasawa Soichi,Nakase Hiroshi,Ozaki Yoshinao,Uza Norimitsu,Matsuura Minoru,Chiba Tsutomu
  • The Lancet 380(9858), 2052-2052, 2012-12-00
  • … 投稿時のタイトルは "Familial Mediterranean Fever with Colonic Involvement Mimicking Inflammatory Bowel Disease" …
  • NAID 120005083813


Familial Mediterranean fever is a disorder passed down through families (inherited), which involves repeated fevers and inflammation that often affects ... Causes Familial Mediterranean fever is most often caused by a ...
Familial Mediterranean Fever Definition Familial Mediterranean fever (FMF) is an inherited disorder of the inflammatory response characterized by recurring attacks of fever, accompanied by intense pain in the abdomen, chest, or ...


Familial Mediterranean FeverFamilial Mediterranean fever. Causes Familial Mediterranean FeverFamilial mediterranean feverFamilial Mediterranean feverFamilial Mediterranean fever | Infectious

先読みRP」「家族性地中海熱」「recurrent polyserositis
関連記事familial」「fever」「Mediterranean」「fevered」「familial mediterranean fever





familial mediterranean fever

recurrent polyserositis」

  [★] 再発性多発漿膜炎



recurrent polyserositis RP
家族性地中海熱 familial Mediterranean fever家族性発作性多発漿膜炎 familial paroxysmal polyserositis、良性発作性多発漿膜炎 benign paroxysmal polyserositis、アルメニア病 Armenian disease


  [★] 再発性多発漿膜炎 recurrent polyserositis RP = 家族性地中海熱, familial Mediterranean fever



  • adj.
  • 家族性の、家系性の、家族の
familyfamily memberhouseholdkindred

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「relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"」

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「家族の,家族特有の / 違伝的な,血統にあらわれる」

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「occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features"」
genetic, hereditary, inherited, transmitted, transmissible



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「a rise in the temperature of the body; frequently a symptom of infection」
febrility, febricity, pyrexia, feverishness

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「intense nervous anticipation; "in a fever of resentment"」

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「〈U〉《しばしばa fever》(身体の異常な)『熱』,発熱 / 〈U〉『熱病』 / 〈U〉〈C〉(…に対する)『興奮』,熱狂《+『for』+『名』》」



  • adj.
  • 地中海の

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「of or relating to or characteristic of or located near the Mediterranean Sea; "Mediterranean countries"」

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「the largest inland sea; between Europe and Africa and Asia」
Mediterranean Sea

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「=Mediterranean Sea / 地中海地方 / 『地中海の』;地中海地方[の住民]特有の」



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「highly excited; "a fevered imagination"」

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「(比較変化なし)《名詞の前にのみ用いて》熱のある,熱病にかかった / 熱にうかされたような,興奮した / (憎しみなどが)異常に強い」

familial mediterranean fever」



hereditary periodic fever syndromeperiodic disease