Literature DB >> 18388145

Autoinflammatory diseases: an update of clinical and genetic aspects.

Q Yao1, D E Furst.   

Abstract

To review clinical manifestations and genetic features of the autoinflammatory diseases, a group of rare, genetically defined diseases which have been newly grouped into a coherent whole. We performed a literature review using the keywords 'periodic fever syndrome', 'autoinflammatory disease' and 'therapy'. All relevant original and review articles in English were reviewed. A case report of each autoinflammatory disease was excerpted from the literature and presented. This review summarizes the clinical manifestations, genetic analysis and therapy of FMF, TNF-alpha receptor-associated periodic fever syndrome, hyperimmunoglobulinaemia D periodic fever syndrome and cryopyrin-associated periodic fever syndrome. These diseases have periodic fever, are hereditary and recurrent, with elevated acute-phase reactants. Differentiating features of these disorders are tabulated. Autoinflammatory diseases have some communalities in their presentation although they represent a relatively diverse group of genetically associated diseases.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18388145     DOI: 10.1093/rheumatology/ken118

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  19 in total

Review 1.  Periodontal and other oral manifestations of immunodeficiency diseases.

Authors:  M E Peacock; R M Arce; C W Cutler
Journal:  Oral Dis       Date:  2016-10-10       Impact factor: 3.511

2.  Rilonacept (arcalyst), an interleukin-1 trap for the treatment of cryopyrin-associated periodic syndromes.

Authors:  Saloni Kapur; Mary Ellen Bonk
Journal:  P T       Date:  2009-03

3.  Coexistent tumor necrosis factor receptor-associated periodic fever syndrome and Ehlers-Danlos syndrome.

Authors:  Qingping Yao; Lan Zhou; Kenneth J Tomecki
Journal:  Rheumatol Int       Date:  2011-07-23       Impact factor: 2.631

Review 4.  Protein misfolding and dysregulated protein homeostasis in autoinflammatory diseases and beyond.

Authors:  Amma F Agyemang; Stephanie R Harrison; Richard M Siegel; Michael F McDermott
Journal:  Semin Immunopathol       Date:  2015-05-21       Impact factor: 9.623

5.  Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes.

Authors:  R Sighart; J Rech; A Hueber; N Blank; S Löhr; A Reis; H Sticht; U Hüffmeier
Journal:  Rheumatol Int       Date:  2017-11-20       Impact factor: 2.631

6.  Trace element levels in patients with familial mediterranean Fever.

Authors:  Kadir Yildirim; Hulya Uzkeser; Abdullah Uyanik; Saliha Karatay; Ahmet Kiziltunc
Journal:  Eurasian J Med       Date:  2011-08

Review 7.  Molecular genetic analysis for periodic fever syndromes: a supplemental role for the diagnosis of adult-onset Still's disease.

Authors:  Hongbin Li; Irina Abramova; Sandra Chesoni; Qingping Yao
Journal:  Clin Rheumatol       Date:  2018-06-17       Impact factor: 2.980

8.  MEFV, TNF1rA, CARD15 and NLRP3 mutation analysis in PFAPA.

Authors:  Efrat Dagan; Ruth Gershoni-Baruch; Ihab Khatib; Adi Mori; Riva Brik
Journal:  Rheumatol Int       Date:  2009-07-05       Impact factor: 2.631

Review 9.  Rare monogenetic syndromes in rheumatology practice.

Authors:  K Manger; H Nüsslein; G Schett; B Manger
Journal:  Clin Rheumatol       Date:  2009-02-18       Impact factor: 2.980

10.  A monoallelic double mutation as a cause for TNF receptor-associated periodic fever syndrome.

Authors:  J Trübenbach; G Wildhardt; J Niebel; H Hawle; Daniela Steinberger
Journal:  Rheumatol Int       Date:  2009-06-23       Impact factor: 2.631

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.