Recent advances in primary Sjogren's syndrome
نویسندگان
چکیده
منابع مشابه
Primary Sjogrens Syndrome in a Child
Sjögren syndrome is uncommon in children and occurs most often in association with autoimmune diseases (secondary Sjögren syndrome). We describe the clinical and biological features of a 7-year-old girl with primary Sjögren syndrome revealed by recurrent parotiditis. CASE REPORT A 7-year-old girl was referred for investigation of multiple episodes of parotid swelling since age 4 years, withou...
متن کاملRecent advances in primary Sjogren's syndrome
Primary Sjögren's syndrome, a chronic inflammatory process, is among the most commonly occurring rheumatologic diseases. The clinical hallmark of this disease is exocrine gland dysfunction, resulting predominately in dry eyes and dry mouth. However, the disease often extends beyond the exocrine glands to seriously affect other organs systems, such as the lungs, kidneys, and nervous system. More...
متن کامل3431 Conjunctiva immunopathology in primary sjogrens syndrome (1° S.S.)
Aim: To evaluate the histological changes and immune response of conjuctiva in patients (pts) with lo S.S. Materials and Methods: We studied conjunctiial biopsies from 15 pts with I0 S.S. and 2 normal controls using 1) paraflfn section screening for the quality of conjunctival epithelium (CE), the number of goblet cells (GC) and the degree of inflammation, 2) Mo-abs and Pabs to: Tlymphocytes, T...
متن کاملRECENT ADVANCES Advances in haemolytic uraemic syndrome
The purpose of this review is to draw together recent advances in the pathogenesis of haemolytic uraemic syndrome (HUS) induced by verocytotoxin, including information from the successful Third International Symposium on Verocytotoxin Producing Escherichia coli, “VTEC’97”, in Baltimore.However, the highly publicised outbreaks of verocytotoxin producing Escherichia coli (VTEC) infection in Japan...
متن کاملRecent Advances in Hemophilia Gene Therapy
Heterogeneous loss of function mutations at F8 and F9 genes causes X-linked recessive bleeding disorders, hemophilia A (HA) and hemophilia B (HB), respectively. HA is clinically indistinguishable from HB and accounts for more than 80% of hemophilia cases; the former affects 1/5000 and the latter 1/25000 male births worldwide. In Iran, it is estimated that around 4300 HA and 900 HB patients are ...
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ژورنال
عنوان ژورنال: F1000Research
سال: 2016
ISSN: 2046-1402
DOI: 10.12688/f1000research.8352.1