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.
Concept/Terms
Familial Mediterranean Fever- Familial Mediterranean Fever
- Periodic Disease
- Disease, Periodic
- Diseases, Periodic
- Periodic Diseases
- Periodic Disease, Wolff's
- Disease, Wolff's Periodic
- Periodic Disease, Wolff
- Periodic Disease, Wolffs
- Wolff's Periodic Disease
- Wolffs Periodic Disease
- Recurrent Polyserositis
- Polyserositides, Recurrent
- Polyserositis, 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
- Familial Paroxysmal Polyserositis
- Familial Paroxysmal Polyserositides
- Paroxysmal Polyserositides, Familial
- Paroxysmal Polyserositis, Familial
- Polyserositides, Familial Paroxysmal
- Polyserositis, Familial Paroxysmal
- Mediterranean Fever, Familial
- Periodic Peritonitis
- Periodic Peritonitides
- Peritonitides, Periodic
- Peritonitis, Periodic
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 Harvard Catalyst Profiles by year, and whether "Familial Mediterranean Fever" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 |
| 1996 | 1 | 1 | 2 |
| 1997 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2006 | 2 | 0 | 2 |
| 2008 | 1 | 0 | 1 |
| 2009 | 2 | 1 | 3 |
| 2010 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 2 | 1 | 3 |
| 2015 | 0 | 1 | 1 |
| 2016 | 4 | 1 | 5 |
| 2018 | 4 | 3 | 7 |
| 2019 | 1 | 1 | 2 |
| 2020 | 1 | 0 | 1 |
| 2021 | 3 | 0 | 3 |
| 2022 | 1 | 0 | 1 |
Below are the most recent publications written about "Familial Mediterranean Fever" by people in Profiles.
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Features predicting colchicine efficacy in treatment of children with undefined systemic autoinflammatory disease: A retrospective cohort study. Eur J Rheumatol. 2022 07; 9(3):116-121.
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Granulocyte-macrophage colony-stimulating factor and tumor necrosis factor-a in combination is a useful diagnostic biomarker to distinguish familial Mediterranean fever from sepsis. Arthritis Res Ther. 2021 10 15; 23(1):260.
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Microbiome is not linked to clinical disease severity of familial Mediterranean fever in an international cohort of children. Clin Exp Rheumatol. 2021 Sep-Oct; 39 Suppl 132(5):102-108.
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Neonatal-Onset Familial Mediterranean Fever in an Infant with Human Parainfluenza Virus-4 Infection. Neonatology. 2021; 118(3):359-363.
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Next-generation sequencing of the whole MEFV gene in Japanese patients with familial Mediterranean fever: a case-control association study. Clin Exp Rheumatol. 2020 Sep-Oct; 38 Suppl 127(5):35-41.
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Successful hydroxychloroquine treatment for familial Mediterranean fever in a Japanese patient with concurrent systemic lupus erythematosus. Rheumatology (Oxford). 2020 04 01; 59(4):903-905.
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Classification criteria for autoinflammatory recurrent fevers. Ann Rheum Dis. 2019 08; 78(8):1025-1032.
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Vertebral artery dissection associated with familial Mediterranean fever and Behçet's disease. Ann Clin Transl Neurol. 2019 May; 6(5):974-978.
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Atypical Familial Mediterranean Fever Complicated with Gastrointestinal Amyloidosis Diagnosed due to Paroxysmal Arthralgia and Intractable Diarrhea, Successfully Treated with Tocilizumab. Intern Med. 2019 Jun 15; 58(12):1781-1785.
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The application of precision medicine in diagnosing familial Mediterranean fever. Leuk Lymphoma. 2019 08; 60(8):2091-2093.