Abstract
Primary IgA nephropathy is characterized by the presence of IgA at the mesangium level accompanied or not by other immunoglobulins in the absence of systemic liver disease. A similar immunofluorescence pattern has been observed in an array of diseases involving mucosal surfaces and the term syndrome of IgA nephropathy has been suggested [1].
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Egido, J. (1987). The Role of Polymeric IgA in the Pathogenesis of IgA Nephropathy. In: Clarkson, A.R. (eds) IgA Nephropathy. Topics in Renal Medicine, vol 2. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2039-5_11
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DOI: https://doi.org/10.1007/978-1-4613-2039-5_11
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