Familial mediterranean fever classification: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 6: | Line 6: | ||
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
|
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.