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Collagenofibrotic glomerulopathy is a rare renal disease, first described by Arakawa in 1979. Fewer than 50 cases have been reported in literature. It occurs more frequently in adult Indian population in a sporadic manner. In normal human kidney, type III collagen is present in the interstitium and blood vessels. Collagenofibrotic glomerulopathy is characterised by accumulation of type III collagen in the glomerular mesangial and subendothelial areas.
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Sawhney et al. (2024) studied this question.
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