Immunotactoid glomerulopathy (ITG) is a very rare condition characterized by glomerular accumulation of microtubules in the mesangium and the glomerular basement membrane, that mainly presents with proteinuria, micro-hematuria, nephrotic syndrome, renal insufficiency and hematologic malignancy. ITG and non-amyloid fibrillary glomerulopathy (non-amyloid FGP) are often grouped together as pathogenetically related diseases.
Comprehensive, easy-to-understand information about this condition
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acute poststreptococcal glomerulonephritis
MONDO:0001870
membranoproliferative glomerulonephritis
MONDO:0002461
exudative glomerulonephritis
MONDO:0003133
proliferative glomerulonephritis
MONDO:0003134
focal embolic glomerulonephritis
MONDO:0003135
anti-basement membrane glomerulonephritis
MONDO:0003136