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									<identifier>oai:www.peertechzpublications.org:10.17352/raoa.000005</identifier>
									<datestamp>2017-03-23</datestamp>
									<setSpec>PTZ.RAOA:VOL1</setSpec>
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										<dc:title>
										IgA Nephropathy Precedes the Onset of the Rheumatic Disease in a Female with Ankylosing Spondylitis
										</dc:title><dc:creator>Haider M Al Attia</dc:creator><dc:creator>Mariano R Carballo</dc:creator><dc:description>&lt;p&gt;IgA nephropathy (known as Berger’s disease) is the most common cause of glomerulonephritis. Its estimated prevalence between 25-50 cases per 100.000 individuals. Gross hematuria (40-50%) and microscopic hematuria (30-40%) are the most common fi ndings which can be related to upper respiratory&lt;/p&gt;&lt;p&gt;tract or gastrointestinal infection. Between 15-40% of affected individuals may progress to chronic renal failure [1-5]. The defi nitive diagnosis is made by renal biopsy fi ndings which is characterized by&amp;nbsp; mesangial IgA deposition. Although the condition is a limited non-systemic renal disease, some systemic diseases are sporadically associated with mesangial IgA deposition. Henoch-Schonlen purpura (HSP), systemic lupus erythematosus (SLE), hepatitis, dermatitis herpetiformis, celiac disease and ankylosing spondylitis ( AS) have been closely linked to the IgA nephropathy [6,7].&lt;/p&gt;</dc:description>
										<dc:publisher>Rheumatica Acta: Open Access - Peertechz Publications</dc:publisher>
										<dc:date>2017-03-23</dc:date>
										<dc:type>Case Report</dc:type>
										<dc:identifier>https://doi.org/10.17352/raoa.000005</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Haider M Al Attia et al.</dc:rights>
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