Auto-inflammatory syndromes and oral health.
Auto-inflammatory diseases (periodic syndromes) are rare childhood-onset disorders which are characterized by fluctuating or recurrent episodes of fever and inflammation affecting serosal surfaces, joints, eyes and/or skin without significant autoantibody production or an identifiable underlying inf...
| Publicado en: | Oral Diseases Vol. 14; no. 8; pp. 690 - 700 |
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| Autores principales: | , , |
| Formato: | review tables/charts Journal Article |
| Publicado: |
Wiley-Blackwell
Nov2008
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=105707185&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 105707185 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 1354523X DZP jtl: Oral Diseases issn: 1354523X maglogo: Y pubinfo: dt: Nov2008 vid: 14 iid: 8 pid: 480 pub: Wiley-Blackwell place: Malden, Massachusetts artinfo: ui: 105707185 2010076766 10.1111/j.1601-0825.2008.01484.x NLM19193198 105707185 ppf: 690 ppct: 10 formats: tig: atl: Auto-inflammatory syndromes and oral health. aug: au: Scully C Hodgson T Lachmann H affil: UCL Eastman Dental Institute, 256 Gray's Inn Road, London WC1X 8LD, UK; crispian.scully@eastman.ucl.ac.uk sug: subj: Amyloidosis Autoimmune Diseases Oral Health Osteomyelitis Stomatitis, Aphthous Fever Genetics Immune System Interleukins Mutation Tumor Necrosis Factor United Kingdom ab: Auto-inflammatory diseases (periodic syndromes) are rare childhood-onset disorders which are characterized by fluctuating or recurrent episodes of fever and inflammation affecting serosal surfaces, joints, eyes and/or skin without significant autoantibody production or an identifiable underlying infection. They are disorders of innate immunity and the underlying genetic defect has been identified in most of the syndromes. Diagnosis relies on clinical symptoms and evidence of an elevated acute phase response during attacks, supported by finding mutations in the relevant genes. Several syndromes can lead to systemic AA amyloidosis. Aphthous-like oral ulceration has been reported as one manifestation in several of the syndromes, including periodic fever, aphthous-stomatitis, pharyngitis, adenitis (PFAPA) familial Mediterranean fever (FMF), hyperimmunoglobulinaemia D and periodic fever syndrome, tumour necrosis factor receptor associated periodic syndrome and pyogenic sterile arthritis, pyoderma gangrenosum, acne (PAPA). Chronic jaw recurrent osteomyelitis has been recorded in chronic recurrent multifocal osteomyelitis. Advances in the molecular pathogenesis of these syndromes and the regulation of innate immunity have enhanced diagnosis, and rationalized therapies. This article reviews the periodic fever syndromes relevant to oral health and the suggested association of FMF with Behçet's disease. pubtype: Academic Journal doctype: review tables/charts Journal Article ougenre: Article language: English refInfo: holdings: @attributes: islocal: N |
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