WordNet
- a unit of geological time during which a system of rocks formed; "ganoid fishes swarmed during the earlier geological periods" (同)geological period
- (ice hockey) one of three divisions into which play is divided in hockey games
- the end or completion of something; "death put a period to his endeavors"; "a change soon put a period to my tranquility"
- the interval taken to complete one cycle of a regularly repeating phenomenon
- a punctuation mark (.) placed at the end of a declarative sentence to indicate a full stop or after abbreviations; "in England they call a period a stop" (同)point, full_stop, stop, full point
- happening or recurring at regular intervals; "the periodic appearance of the seventeen-year locust" (同)periodical
- recurring or reappearing from time to time; "periodic feelings of anxiety" (同)occasional
- a rise in the temperature of the body; frequently a symptom of infection (同)febrility, febricity, pyrexia, feverishness
- intense nervous anticipation; "in a fever of resentment"
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- highly excited; "a fevered imagination"
PrepTutorEJDIC
- (あることが続く)『期間』 / (歴史的な)『時代』 / (試合の)『一区切り』,ピリオド / 授業時間,時限: / (循環して起こる現象などの)周期 / (回転運動などの)周期 / 紀(地質時代の区分の一つ;era(代)の下,epoch(世)の上) / 《おもに米》『ピリオド』,終止符(《英》full stop;Mr.,U.S.など略語の符号(.)も含む) / 《複数形で》《文》掉尾(とうび)文(多くの節から成り,論理的に緊密な構成をもっている文) / 《名詞の前にのみ用いて》ある時代[特有]の,時代物の / (文の終わりに感嘆詞的に)以上,終わり・月経(期間)
- 定期的な,周期的な / ときぎき起こる: / 掉尾(とうび)的の:
- 〈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』》
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
- (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
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2012/12/23 14:10:35」(JST)
[Wiki en表示]
Periodic fever syndrome |
Classification and external resources |
ICD-10 |
E85.0 |
ICD-9 |
277.31 |
DiseasesDB |
9836 |
eMedicine |
article/952254 |
MeSH |
D056660 |
The periodic fever syndromes (also known as autoinflammatory syndromes) are a set of disorders, many of which are genetic disorders in which the mechanisms which initiate and control inflammation are disturbed, leading to uncontrolled inflammation throughout the body. The syndromes are diverse, but tend to cause fever, joint pains, abdominal pains and may lead to chronic complications such as amyloidosis.[1]
Restated, autoinflammatory syndromes are a group of inherited disorders characterized by bouts of inflammatory skin lesions and periodic fevers.[2]:148
Periodic fever syndromes are medically distinct from immunodeficiency conditions, in which infections can occur frequently and induce fever.
Individual periodic fever syndromes
Name |
OMIM |
Gene |
Familial Mediterranean fever (FMF) |
249100 |
MEFV |
Hyperimmunoglobulinemia D with recurrent fever (HIDS). This is now (along with mevalonic aciduria) defined as a mevalonate kinase deficiency[3] |
260920 |
MVK |
TNF receptor associated periodic syndrome (TRAPS) |
142680 |
TNFRSF1A |
CAPS: Muckle-Wells syndrome (urticaria deafness amyloidosis) |
191900 |
NLRP3 |
CAPS: Familial cold urticaria |
120100 |
NLRP3 |
CAPS: Neonatal onset multisystem inflammatory disease (NOMID) |
607115 |
NLRP3 |
Periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA syndrome) |
none |
? |
Blau syndrome |
186580 |
NOD2 |
Pyogenic sterile arthritis, pyoderma gangrenosum, acne (PAPA) |
604416\ |
PSTPIP1 |
Deficiency of the interleukin-1–receptor antagonist (DIRA) |
612852 |
IL1RN |
References
- ^ Stojanov S, Kastner DL (2005). "Familial autoinflammatory diseases: genetics, pathogenesis and treatment". Curr Opin Rheumatol 17 (5): 586–99. doi:10.1097/bor.0000174210.78449.6b. PMID 16093838.
- ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
- ^ Houten SM, Frenkel J, Waterham HR (2003). "Isoprenoid biosynthesis in hereditary periodic fever syndromes and inflammation". Cell. Mol. Life Sci. 60 (6): 1118–34. doi:10.1007/s00018-003-2296-4. PMID 12861380.
See also
- List of cutaneous conditions
The autoinflammatory syndromes are of crucial importance for immunology in general. These syndromes actually define diseases that are driven by the innate immune system. Therefore, these conditions define the diametric genetic and immunopathological opposites of the classical autoimmune diseases that are driven by B and T cells. These diseases actually define one boundary of the immulological disease continuum of inflammation against self.
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- Treatment of hereditary autoinflammatory diseases.
- Ter Haar NM1, Frenkel J.Author information 1aDepartment of Pediatric Rheumatology bDepartment of General Pediatrics, University Medical Center Utrecht, Utrecht, The Netherlands.AbstractPURPOSE OF REVIEW: The purpose of this review is to summarize recent advances in the treatment of the hereditary autoinflammatory diseases, focusing on Familial Mediterranean fever (FMF), tumor necrosis factor receptor-associated periodic syndrome (TRAPS), cryopyrin-associated periodic syndromes (CAPS) and mevalonate kinase deficiency (MKD). We discuss recently published studies and their implications for current patient care and future clinical research.
- Current opinion in rheumatology.Curr Opin Rheumatol.2014 May;26(3):252-8. doi: 10.1097/BOR.0000000000000059.
- PURPOSE OF REVIEW: The purpose of this review is to summarize recent advances in the treatment of the hereditary autoinflammatory diseases, focusing on Familial Mediterranean fever (FMF), tumor necrosis factor receptor-associated periodic syndrome (TRAPS), cryopyrin-associated periodic syndromes (CA
- PMID 24667287
- Periodic fevers in adult Greeks: clinical and molecular presentation.
- Karatsourakis TP1, Oikonomaki KN, Tzioufas AG, Moutsopoulos HM.Author information 1Department of Pathophysiology, School of Medicine, University of Athens, Athens 11527, Greece. karatsourakis@yahoo.gr.AbstractOBJECTIVES: Hereditary periodic fever syndromes (HPFS) are rare diseases characterised by recurrent, self-limited episodes of fever and localised inflammation, which arise from monogenic defects. In the present study we describe the clinical features, laboratory parameters and genetic profile of adult patients.
- Clinical and experimental rheumatology.Clin Exp Rheumatol.2014 Apr 7. [Epub ahead of print]
- OBJECTIVES: Hereditary periodic fever syndromes (HPFS) are rare diseases characterised by recurrent, self-limited episodes of fever and localised inflammation, which arise from monogenic defects. In the present study we describe the clinical features, laboratory parameters and genetic profile of adu
- PMID 24708999
- A157: Macrophage Activation Syndrome-like Illness Due to an Activating Mutation in NLRC4.
- Canna S1, de Jesus AA, Deng Z, Gouni S, Marrero B, Brooks S, Dimattia M, Liu Y, Huang Y, Plass N, Chapelle DC, Montealegre G, Benseler S, Laxer RM, Goldbach-Mansky R.Author information 1NIAMS/NIH, Bethesda, MD.AbstractBACKGROUND/PURPOSE: Macrophage Activation Syndrome (MAS) is a life-threatening systemic inflammatory disorder of unknown etiology. While MAS has no known genetic basis, clinical similarity with a genetic disorder of impaired cytotoxicity known as primary Hemophagocytic Lymphohistiocytosis (HLH) has suggested shared pathogenesis. In contrast, other investigations have suggested innate immune dysregulation drives MAS.
- Arthritis & rheumatology (Hoboken, N.J.).Arthritis Rheumatol.2014 Mar;66 Suppl 11:S203. doi: 10.1002/art.38583.
- BACKGROUND/PURPOSE: Macrophage Activation Syndrome (MAS) is a life-threatening systemic inflammatory disorder of unknown etiology. While MAS has no known genetic basis, clinical similarity with a genetic disorder of impaired cytotoxicity known as primary Hemophagocytic Lymphohistiocytosis (HLH) has
- PMID 24677912
Japanese Journal
- Variable intrafamilial expressivity of the rare tumor necrosis factor-receptor associated periodic syndrome-associated mutation I170N that affects the TNFR1A cleavage site
- LEHMANN Petra,SALZBERGER Bernd,HAERLE Peter,AKSENTIJEVICH Ivona,KASTNER Daniel,SCHOELMERICH Juergen,ROSENFELD Stephanie,MUELLER-LADNER Ulf
- Modern rheumatology 20(3), 311-315, 2010-06-01
- NAID 10027169540
Related Links
- 11 Jan 2013 ... Background. Hereditary periodic fever syndromes (HPFSs) are rare and distinct heritable disorders characterized by short and recurrent attacks of fever and severe localized inflammation that occur periodically or irregularly ...
- The periodic fever syndromes (also known as autoinflammatory syndromes) are a set of disorders, many of which are genetic disorders in which the mechanisms which initiate and control inflammation are disturbed, leading to uncontrolled ...
Related Pictures
★リンクテーブル★
[★]
- 関
- familial mediterranean fever、hereditary periodic fever syndrome
[★]
- 英
- hereditary periodic fever syndrome
- 関
- 家族性地中海熱、周期性疾患
[★]
家族性地中海熱
- 関
- hereditary periodic fever syndrome、periodic disease
[★]
- 周期的な、(天)周期運動をする、周期手金あ。定期の、定時の。間欠的な、断続的な。
- 関
- cyclic, cyclical, cyclically, cyclicity, periodical, periodically, periodicity, regular, regularly, rhythmic
[★]
- 関
- heredity、heritable、inherit、inheritable、inheritable character、inheritance、inherited
[★]
- 関
- duration、phase、stage、term、time
[★]