Familial mediterranean fever classification: Difference between revisions
(Created page with "__NOTOC__ {{Familial mediterranean fever}} {{CMG}}; {{AE}} {{Sahar}} ==Overview== There is no established system for the classification of familial Mediterranean fever. Howev...") |
No edit summary |
||
| Line 4: | Line 4: | ||
{{CMG}}; {{AE}} {{Sahar}} | {{CMG}}; {{AE}} {{Sahar}} | ||
==Overview== | ==Overview== | ||
There is no established system for the classification of familial Mediterranean fever. However, familial Mediterranean fever may be classified according to phenotypic manifestation into three subtypes/groups: type 1, type 2, and type 3. | There is no established system for the [[classification]] of [[familial Mediterranean fever]]. However, [[familial Mediterranean fever]] may be classified according to [[Phenotype|phenotypic]] manifestation into three subtypes/groups: type 1, type 2, and type 3. | ||
==Classification== | ==[[Classification]]== | ||
There is no established system for the classification of familial Mediterranean fever. However, familial Mediterranean fever may be classified according to phenotypic manifestation into three subtypes/groups:<ref name="ProcopioManti2018">{{cite journal|last1=Procopio|first1=V.|last2=Manti|first2=S.|last3=Bianco|first3=G.|last4=Conti|first4=G.|last5=Romeo|first5=A.|last6=Maimone|first6=F.|last7=Arrigo|first7=T.|last8=Cutrupi|first8=M.C.|last9=Salpietro|first9=C.|last10=Cuppari|first10=C.|title=Genotype-phenotype correlation in FMF patients: A “non classic” recessive autosomal or “atypical” dominant autosomal inheritance?|journal=Gene|volume=641|year=2018|pages=279–286|issn=03781119|doi=10.1016/j.gene.2017.10.068}}</ref> | There is no established system for the [[classification]] of [[familial Mediterranean fever]]. However, [[Familial mediterranean fever|familial Mediterranean fever]] may be classified according to [[phenotypic]] manifestation into three subtypes/groups:<ref name="ProcopioManti2018">{{cite journal|last1=Procopio|first1=V.|last2=Manti|first2=S.|last3=Bianco|first3=G.|last4=Conti|first4=G.|last5=Romeo|first5=A.|last6=Maimone|first6=F.|last7=Arrigo|first7=T.|last8=Cutrupi|first8=M.C.|last9=Salpietro|first9=C.|last10=Cuppari|first10=C.|title=Genotype-phenotype correlation in FMF patients: A “non classic” recessive autosomal or “atypical” dominant autosomal inheritance?|journal=Gene|volume=641|year=2018|pages=279–286|issn=03781119|doi=10.1016/j.gene.2017.10.068}}</ref> | ||
*Type 1: this type is manifested with recurrent short episodes of inflammation and serositis. | *Type 1: this type is manifested with recurrent short episodes of [[inflammation]] and [[serositis]]. | ||
*Type 2: Amyloidosis represents the first clinical manifestation of the disease in an otherwise asymptomatic individual | *Type 2: [[Amyloidosis]] represents the first clinical manifestation of the [[disease]] in an otherwise [[asymptomatic]] individual | ||
*Type 3: characterized by two MEFV mutations detection in asymptomatic patients. | *Type 3: characterized by two [[MEFV]] [[mutations]] detection in [[asymptomatic]] [[patients]]. | ||
==References== | ==References== | ||
Revision as of 16:39, 30 May 2019
|
Familial Mediterranean Fever Microchapters |
|
Differentiating Familial Mediterranean Fever from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Familial mediterranean fever classification On the Web |
|
American Roentgen Ray Society Images of Familial mediterranean fever classification |
|
Directions to Hospitals Treating Familial mediterranean fever |
|
Risk calculators and risk factors for Familial mediterranean fever classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2]
Overview
There is no established system for the classification of familial Mediterranean fever. However, familial Mediterranean fever may be classified according to phenotypic manifestation into three subtypes/groups: type 1, type 2, and type 3.
Classification
There is no established system for the classification of familial Mediterranean fever. However, familial Mediterranean fever may be classified according to phenotypic manifestation into three subtypes/groups:[1]
- Type 1: this type is manifested with recurrent short episodes of inflammation and serositis.
- Type 2: Amyloidosis represents the first clinical manifestation of the disease in an otherwise asymptomatic individual
- Type 3: characterized by two MEFV mutations detection in asymptomatic patients.
References
- ↑ Procopio, V.; Manti, S.; Bianco, G.; Conti, G.; Romeo, A.; Maimone, F.; Arrigo, T.; Cutrupi, M.C.; Salpietro, C.; Cuppari, C. (2018). "Genotype-phenotype correlation in FMF patients: A "non classic" recessive autosomal or "atypical" dominant autosomal inheritance?". Gene. 641: 279–286. doi:10.1016/j.gene.2017.10.068. ISSN 0378-1119.