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.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Familial Mediterranean Fever" by people in Profiles.
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Mangan MSJ, Gorki F, Krause K, Heinz A, Pankow A, Ebert T, Jahn D, Hiller K, Hornung V, Maurer M, Schmidt FI, Gerhard R, Latz E. Transcriptional licensing is required for Pyrin inflammasome activation in human macrophages and bypassed by mutations causing familial Mediterranean fever. PLoS Biol. 2022 11; 20(11):e3001351.
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Humphries F, Shmuel-Galia L, Ketelut-Carneiro N, Li S, Wang B, Nemmara VV, Wilson R, Jiang Z, Khalighinejad F, Muneeruddin K, Shaffer SA, Dutta R, Ionete C, Pesiridis S, Yang S, Thompson PR, Fitzgerald KA. Succination inactivates gasdermin D and blocks pyroptosis. Science. 2020 09 25; 369(6511):1633-1637.
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Philips BH, Loria KO, Sirivelu MP, Jaber SM, Allen-Worthington KH, Veeder CL, Brice AK. Pathology in Practice. J Am Vet Med Assoc. 2016 Oct 01; 249(7):755-7.
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Akula MK, Shi M, Jiang Z, Foster CE, Miao D, Li AS, Zhang X, Gavin RM, Forde SD, Germain G, Carpenter S, Rosadini CV, Gritsman K, Chae JJ, Hampton R, Silverman N, Gravallese EM, Kagan JC, Fitzgerald KA, Kastner DL, Golenbock DT, Bergo MO, Wang D. Control of the innate immune response by the mevalonate pathway. Nat Immunol. 2016 08; 17(8):922-9.
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Wiseman DH, May A, Jolles S, Connor P, Powell C, Heeney MM, Giardina PJ, Klaassen RJ, Chakraborty P, Geraghty MT, Major-Cook N, Kannengiesser C, Thuret I, Thompson AA, Marques L, Hughes S, Bonney DK, Bottomley SS, Fleming MD, Wynn RF. A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD). Blood. 2013 Jul 04; 122(1):112-23.
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John CC, Schreiber JR. The revolution in molecular biology leads to new understanding of the clinical expression of immunodeficiencies. J Pediatr. 2003 Feb; 142(2):99-101.