Familial Mediterranean Fever
"Familial Mediterranean Fever" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease.
| Descriptor ID |
D010505
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| MeSH Number(s) |
C16.320.382.625
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| Concept/Terms |
Familial Mediterranean Fever- Familial Mediterranean Fever
- Familial Mediterranean Fever, Autosomal Recessive
- Familial Paroxysmal Polyserositis
- Familial Paroxysmal Polyserositides
- Paroxysmal Polyserositides, Familial
- Paroxysmal Polyserositis, Familial
- Polyserositides, Familial Paroxysmal
- Mediterranean Fever, Familial
- Periodic Disease
- Disease, Periodic
- Diseases, Periodic
- Periodic Diseases
- Wolff's Periodic Disease
- Wolffs Periodic Disease
- Periodic Peritonitis
- Periodic Peritonitides
- Peritonitides, Periodic
- Peritonitis, Periodic
- Polyserositis, Familial Paroxysmal
- Polyserositis, Recurrent
- Recurrent Polyserositis
- Polyserositides, Recurrent
- Recurrent Polyserositides
- Wolff Periodic Disease
- Disease, Wolff Periodic
- Benign Paroxysmal Peritonitis
- Benign Paroxysmal Peritonitides
- Paroxysmal Peritonitides, Benign
- Paroxysmal Peritonitis, Benign
- Peritonitides, Benign Paroxysmal
- Peritonitis, Benign Paroxysmal
- Periodic Disease, Wolff's
- Disease, Wolff's Periodic
- Periodic Disease, Wolff
- Periodic Disease, Wolffs
|
Below are MeSH descriptors whose meaning is more general than "Familial Mediterranean Fever".
Below are MeSH descriptors whose meaning is more specific than "Familial Mediterranean Fever".
This graph shows the total number of publications written about "Familial Mediterranean Fever" by people in this website by year, and whether "Familial Mediterranean Fever" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Familial Mediterranean Fever" by people in Profiles.
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Koga T, Sato S, Hagimori N, Yamamoto H, Ishimura M, Yasumi T, Kirino Y, Ikeda K, Yachie A, Migita K, Kishida D, Atsumi T, Kawakami A. A randomised, double-blind, placebo-controlled phase III trial on the efficacy and safety of tocilizumab in patients with familial Mediterranean fever. Clin Exp Rheumatol. 2022 Sep; 40(8):1535-1542.
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Samukawa S, Yoshimi R, Kirino Y, Nakajima H. The PRY/SPRY domain of pyrin/TRIM20 interacts with ß2-microglobulin to promote inflammasome formation. Sci Rep. 2021 12 08; 11(1):23613.
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Kirino Y, Zhou Q, Ishigatsubo Y, Mizuki N, Tugal-Tutkun I, Seyahi E, Özyazgan Y, Ugurlu S, Erer B, Abaci N, Ustek D, Meguro A, Ueda A, Takeno M, Inoko H, Ombrello MJ, Satorius CL, Maskeri B, Mullikin JC, Sun HW, Gutierrez-Cruz G, Kim Y, Wilson AF, Kastner DL, Gül A, Remmers EF. Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease. Proc Natl Acad Sci U S A. 2013 May 14; 110(20):8134-9.
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Yu JW, Fernandes-Alnemri T, Datta P, Wu J, Juliana C, Solorzano L, McCormick M, Zhang Z, Alnemri ES. Pyrin activates the ASC pyroptosome in response to engagement by autoinflammatory PSTPIP1 mutants. Mol Cell. 2007 Oct 26; 28(2):214-27.