Pediatric IgA nephropathy

IgA nephropathy was first described by Berger in 1968. It is a group of glomerular diseases characterized by mesangial proliferation and markedly diffuse IgA deposition in the mesangial area. The clinical manifestations are diverse, with hematuria being the most common. IgA nephropathy can be divided into two types: primary and secondary. The latter is often secondary to diseases such as liver cirrhosis, intestinal disease, arthritis, and herpes dermatitis. It also has significant IgA deposition in the glomerular mesangial area. As a feature. Primary IgA nephropathy is considered to be one of the most common glomerulonephritis in many parts of the world, and it is one of the common causes of end-stage renal failure. This section mainly introduces primary IgA nephropathy.

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