2005
DOI: 10.1007/s00467-005-2060-0
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Our case with IgA deficiency and membranous glomerulonephritis

Abstract: Sirs, I read with interest the Letter to the Editors, "IgA deficiency and membranous glomerulonephritis (MGN)," by Watanabe [1]. Watanabe suggested that the MGN affecting our patient with IgA deficiency and MGN is more likely to have resulted from in site immune complex formation caused by chronic immunological activation or cryptic autoimmune disease than from circulating immune complexes, given the pathological and laboratory findings obtained. I think that the content of the Letter by Watanabe is very impor… Show more

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“…Many of these individuals have no apparent disease, whereas selected patients suffer from recurrent mucosal infections, allergies and autoimmune diseases [2,3,4]. Furthermore, unexplained coincidences between SIgAD and systemic autoimmune disorders such as systemic lupus erythematosus, rheumatoid arthritis, celiac disease, hemolytic anemia, thyroiditis, type 1 diabetes mellitus, juvenile rheumatoid arthritis and autoimmune glomerulonephritis were reported [5,6,7,8,9]. …”
Section: Introductionmentioning
confidence: 99%
“…Many of these individuals have no apparent disease, whereas selected patients suffer from recurrent mucosal infections, allergies and autoimmune diseases [2,3,4]. Furthermore, unexplained coincidences between SIgAD and systemic autoimmune disorders such as systemic lupus erythematosus, rheumatoid arthritis, celiac disease, hemolytic anemia, thyroiditis, type 1 diabetes mellitus, juvenile rheumatoid arthritis and autoimmune glomerulonephritis were reported [5,6,7,8,9]. …”
Section: Introductionmentioning
confidence: 99%