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Sjögren's Syndrome: State of the Art on Clinical Practice Guideline

dc.contributor.authorRomão, V
dc.contributor.authorTalarico, R
dc.contributor.authorScirè, CA
dc.contributor.authorVieira, A
dc.contributor.authorAlexander, T
dc.contributor.authorBaldini, C
dc.contributor.authorGottenberg, JE
dc.contributor.authorGruner, H
dc.contributor.authorHachulla, E
dc.contributor.authorMouthon, L
dc.contributor.authorOrlandi, M
dc.contributor.authorPamfil, C
dc.contributor.authorPineton de Chambrun, M
dc.contributor.authorTaglietti, M
dc.contributor.authorToplak, N
dc.contributor.authorvan Daele, P
dc.contributor.authorvan Laar, JM
dc.contributor.authorBombardieri, S
dc.contributor.authorSchneider, M
dc.contributor.authorSmith, V
dc.contributor.authorCutolo, M
dc.contributor.authorMosca, M
dc.contributor.authorMariette, X
dc.date.accessioned2019-10-11T15:44:14Z
dc.date.available2019-10-11T15:44:14Z
dc.date.issued2018
dc.description.abstractSjögren's syndrome (SS) is a complex autoimmune rheumatic disease that specifically targets salivary and lachrymal glands. As such, patients typically had ocular and oral dryness and salivary gland swelling. Moreover, skin, nasal and vaginal dryness are frequently present. In addition to dryness, musculoskeletal pain and fatigue are the hallmarks of this disease and constitute the classic symptom triad presented by the vast majority of patients. Up to 30% to 50 % of patients with SS may present systemic disease; moreover, there is an increased risk for the development of non-Hodgkin's lymphoma that occurs in a minority of patients. The present work was developed in the framework of the European Reference Network (ERN) dedicated to Rare and Complex Connective Tissue and Musculoskeletal Diseases (ReCONNET). In line with its goals of aiming to improve early diagnosis, treatment and care of rare connective and musculoskeletal diseases, ERN-ReCONNET set to review the current state of clinical practice guidelines (CPGs) in the rare and complex connective tissue diseases of interest of the network. Therefore, the present work was aimed at providing a state of the art of CPGs for SS.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationRMD Open. 2018 Oct 18;4(Suppl 1):e000789.pt_PT
dc.identifier.doi10.1136/rmdopen-2018-000789pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/3332
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherBMJ Publishing Grouppt_PT
dc.subjectHCC MEDpt_PT
dc.subjectSjögren's Syndromept_PT
dc.titleSjögren's Syndrome: State of the Art on Clinical Practice Guidelinept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issueSuppl 1pt_PT
oaire.citation.startPagee000789pt_PT
oaire.citation.titleRMD Openpt_PT
oaire.citation.volume4pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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