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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.
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|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 15:28, 7 June 2019

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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

References

  1. 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.

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