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- W4211002023 startingPage "243" @default.
- W4211002023 abstract "The term Sjogren’s syndrome (SS) refers to xeropthalmia and xerostomia due to lymphocytic infiltrates of lacrimal and salivary glands. The condition may exist as a primary entity (primary SS, 1° SS) or in association with other autoimmune disorders such as systemic lupus erythematosus (SLE), dermatomyositis, scleroderma or rheumatoid arthritis (in which the sicca symptoms are termed “secondary” SS, 2° SS). The criteria for diagnosis of primary SS has been controversial. The absence of a uniformly accepted criteria has led to confusion in clinical practice and in the research literature. For example, only 15% of patients that fulfill European (EEC) criteria for SS would fulfill the San Diego criteria. This difference in disease classification leads to difficulty in comparing clinical trials and in elucidating pathogenetic mechanisms, since different patient populations are evaluated. However, a new international criteria has been suggested and will be presented since the final version of this criteria is close to acceptance by rheumatologists and government agencies.KeywordsSalivary GlandSystemic Lupus Erythematosus PatientCongenital Heart BlockSubacute Cutaneous Lupus ErythematosusSicca SymptomThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves." @default.
- W4211002023 created "2022-02-13" @default.
- W4211002023 creator A5030910537 @default.
- W4211002023 date "2001-01-01" @default.
- W4211002023 modified "2023-09-28" @default.
- W4211002023 title "Sjogren’s Syndrome" @default.
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