 Hereditary Autoinflammatory Diseases
"Hereditary Autoinflammatory Diseases" 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.
Hereditary inflammation conditions, characterized by recurrent episodes of systemic inflammation. Common symptoms include recurrent fever, rash, arthritis, fatigue, and secondary AMYLOIDOSIS. Hereditary autoinflammatory diseases are associated with mutations in genes involved in regulation of normal inflammatory process and are not caused by AUTOANTIBODIES, or antigen specific T-LYMPHOCYTES.
| Descriptor ID |
D056660
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| MeSH Number(s) |
C16.320.382 C17.800.827.368
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| Concept/Terms |
Hereditary Autoinflammatory Diseases- Hereditary Autoinflammatory Diseases
- Autoinflammatory Disease, Hereditary
- Autoinflammatory Diseases, Hereditary
- Disease, Hereditary Autoinflammatory
- Diseases, Hereditary Autoinflammatory
- Hereditary Autoinflammatory Disease
- Hereditary Recurrent Fevers
- Fever, Hereditary Recurrent
- Fevers, Hereditary Recurrent
- Hereditary Recurrent Fever
- Recurrent Fever, Hereditary
- Recurrent Fevers, Hereditary
- Siegal-Cattan-Mamou Disease
- Disease, Siegal-Cattan-Mamou
- Siegal Cattan Mamou Disease
- Reimann Periodic Disease
- Disease, Reimann Periodic
- Diseases, Reimann Periodic
- Periodic Disease, Reimann
- Periodic Diseases, Reimann
- Reimann Periodic Diseases
- Hereditary Autoinflammation Diseases
- Autoinflammation Disease, Hereditary
- Autoinflammation Diseases, Hereditary
- Disease, Hereditary Autoinflammation
- Diseases, Hereditary Autoinflammation
- Hereditary Autoinflammation Disease
- Hereditary Periodic Fever Syndromes
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Below are MeSH descriptors whose meaning is more general than "Hereditary Autoinflammatory Diseases".
Below are MeSH descriptors whose meaning is more specific than "Hereditary Autoinflammatory Diseases".
This graph shows the total number of publications written about "Hereditary Autoinflammatory Diseases" by people in this website by year, and whether "Hereditary Autoinflammatory Diseases" 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 |
|---|
| 2011 | 2 | 0 | 2 | | 2015 | 0 | 1 | 1 | | 2016 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hereditary Autoinflammatory Diseases" by people in Profiles.
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Tyler PM, Bucklin ML, Zhao M, Maher TJ, Rice AJ, Ji W, Warner N, Pan J, Morotti R, McCarthy P, Griffiths A, van Rossum AMC, Hollink IHIM, Dalm VASH, Catanzaro J, Lakhani SA, Muise AM, Lucas CL. Human autoinflammatory disease reveals ELF4 as a transcriptional regulator of inflammation. Nat Immunol. 2021 09; 22(9):1118-1126.
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Sanchez GAM, Reinhardt A, Ramsey S, Wittkowski H, Hashkes PJ, Berkun Y, Schalm S, Murias S, Dare JA, Brown D, Stone DL, Gao L, Klausmeier T, Foell D, de Jesus AA, Chapelle DC, Kim H, Dill S, Colbert RA, Failla L, Kost B, O'Brien M, Reynolds JC, Folio LR, Calvo KR, Paul SM, Weir N, Brofferio A, Soldatos A, Biancotto A, Cowen EW, Digiovanna JJ, Gadina M, Lipton AJ, Hadigan C, Holland SM, Fontana J, Alawad AS, Brown RJ, Rother KI, Heller T, Brooks KM, Kumar P, Brooks SR, Waldman M, Singh HK, Nickeleit V, Silk M, Prakash A, Janes JM, Ozen S, Wakim PG, Brogan PA, Macias WL, Goldbach-Mansky R. JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies. J Clin Invest. 2018 07 02; 128(7):3041-3052.
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Batu ED, Kara Eroglu F, Tsoukas P, Hausmann JS, Bilginer Y, Kenna MA, Licameli GR, Fuhlbrigge RC, ?zen S, Dedeoglu F. Periodic Fever, Aphthosis, Pharyngitis, and Adenitis Syndrome: Analysis of Patients From Two Geographic Areas. Arthritis Care Res (Hoboken). 2016 12; 68(12):1859-1865.
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Cavalli G, Dinarello CA. Treating rheumatological diseases and co-morbidities with interleukin-1 blocking therapies. Rheumatology (Oxford). 2015 Dec; 54(12):2134-44.
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Stenerson M, Dufendach K, Aksentijevich I, Brady J, Austin J, Reed AM. The first reported case of compound heterozygous IL1RN mutations causing deficiency of the interleukin-1 receptor antagonist. Arthritis Rheum. 2011 Dec; 63(12):4018-22.
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Dinarello CA. A clinical perspective of IL-1? as the gatekeeper of inflammation. Eur J Immunol. 2011 May; 41(5):1203-17.
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