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Journal of Indian Academy of Oral Medicine and Radiology, 2011 Sjogren′s syndrome, also known as "Mikulicz disease" or "Sicca syndrome" is a systemic autoimmune disease in which immune cells attack and destroy the exocrine glands that produce tears and saliva. It can exist by itself (primary Sjogren syndrome) or develop in association with another disorder such as rheumatoid arthritis, systemic sclerosis, primary ...
Rani Somani +3 more
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Srpski arhiv za celokupno lekarstvo, 2008 Sjogren's syndrome is a chronic inflammatory disease of unknown aethiology. It is characterized by decreased secretion of salivary and lacrimal glands, which induces keratoconjunctivitis sicca and xerostomia. Sjogren's syndrome is a central autoimmune disease, and it has characteristics of both organ-specific and generalized autoimmune diseases. It can
S, Rasković +3 more
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Anaesthesia for caesarean section in a parturient with sjogren syndrome and scoping review
Journal of Obstetric Anaesthesia and Critical Care, 2023 Sjogren syndrome is a slowly progressive autoimmune disease with lymphocytic infiltration of exocrine glands, peri-epithelial and extra-epithelial tissues.
Shalvi Mahajan +3 more
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Neurological manifestations of Sjogren syndrome: A case series. [PDF]
J Family Med Prim CareThe Sjogren syndrome is known to have a variety of manifestations apart from the classical glandular involvement. These include musculoskeletal, vascular, neurological, gastrointestinal, and renal involvement.
Gupta K +5 more
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Case Report: <i>Streptococcus gordonii</i> triggering suppurative parotitis and sepsis in a patient with Sjögren syndrome. [PDF]
Front Med (Lausanne)BackgroundAcute suppurative parotitis is common in primary Sjögren syndrome due to parotid gland dysfunction. Streptococcus gordonii is an aggressive pathogen but is rarely reported in acute suppurative parotitis.Case summaryA 64-year-old woman with ...
Wang Y +4 more
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Sjogren – Larsson Syndrome [PDF]
Medical Journal Armed Forces India, 2002 Sjogren – Larsson Syndrome (SLS) is a rare neuroectodermal genodermatosis inherited as an autosomal recessive disorder. It seems more common in North Sweden than elsewhere in Europe and has been estimated as having the incidence of 10.2 in 1000,000 [1].
A K, Dubey, R K, Gupta, Arvind, Gupta
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Cerebellar degeneration in primary Sjögren syndrome: a case report
Journal of Medical Case Reports, 2021 Background Cerebellar degeneration is a rare and severe presentation of primary Sjögren syndrome. There are few case reports of cerebellar degeneration associated with different autoimmune diseases, especially with systemic lupus erythematosus and neuro ...
Seow Lin Chuah +3 more
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BMC Rheumatology, 2023 Background Dry eyes and mouth are symptoms of Sjogren syndrome, which can occur on its own and be referred to as primary Sjogren syndrome or in conjunction with other rheumatic diseases like rheumatoid arthritis and be referred to as secondary Sjogren ...
Hagar Elsayed Fakher +3 more
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BMC Nephrology, 2021 Background Acquired Gitelman syndrome is a very rare disorder reported in association with autoimmune disorders, mostly Sjögren syndrome. It is characterized by the presence of hypokalaemic metabolic alkalosis, hypocalciuria, hypomagnesaemia and hyper ...
Rasika Ranaweerage +2 more
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Pediatric Rheumatology Online Journal, 2020 Background Sjögren syndrome (SS) is a rare disease in pediatrics, and little attention has been paid to the clinical feature in these patients. To date, there are few cases concern about neurological and nephrological disorders in childhood Sjögren ...
Jingya Zhao +6 more
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