… Deficiency of FI is a very rare primary immunodeficiency, inherited as an … both pathological
entities, which share common molecular mechanisms … Haemolytic uraemic syndrome …

… of primary GN (like IgA glomerulonephritis, dense deposit disease, C3 glomerulonephritis,
post… that lead to the development of C3GN or to atypical haemolytic uremic syndrome (aHUS). …

… C3 glomerulopathy (C3G) is a clinicopathologic entity … ), and C3 glomerulonephritis (C3GN),
in which deposits may be … immunofluorescence staining for C3, either isolated or at least two …

… C3 glomerulopathies are rare diseases that share an … into dense deposit disease (DDD)
and C3 glomerulonephritis (… of allograft failure in 189,211 primary kidney transplant recipients …

… they could be a continuation of the same entity [3, 4]. Historically, … However, since both
primary and secondary MPGN … , it has been found that isolated C3 deposited idiopathic MPGN-…

… C3 glomerulonephritis (C3GN) and dense deposit disease (… /mL], and there was isolated
depression of C3 at 67 mg/dL [… The importance of both genetic and environmental risk factors …

… with atypical hemolytic and uremic syndrome: genetic complement … C3 glomerulonephritis
and dense deposit disease share a … in nephrotic syndrome due to primary glomerulonephritis. …

… C3 glomerulopathy is a relatively new clinical entity that … pathway activation appears to be
the primary cause of C3G [13] … these C3 glomerulonephritis (C3GN) patients, the C3 deposits …

… and is the underlying primary glomerulopathy in 5–… deposit disease, whereas complement
dysregulation at endothelial surfaces typically leads to atypical haemolytic uraemic syndrome. …

… renal disorders that share certain common histologic features… of differentiating between these
entities for management and … C3 or C4 are classified as primary GN and are defined as C3 …