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. 2020 Dec 30;32(2):268–278. doi: 10.1681/ASN.2020071082

Table 1.

Clinical and pathologic findings

MN Mean Age (yr) Sex (M: F) Laboratory Findings Disease Association Serum Antibody LM IF Complement IgG Subtype EM
EXT1/EXT2-MN (n=26) 36 1:4 ANA, dsDNA, SSA, SSB, others Autoimmune diseases: lupus, MCTD/ No Proliferative features may be present IgG, IgA/IgM C3, C1q IgG1 SE, ME + SU +/− TRI
NELL1-MN (n=34) 63 1:1 Negative Malignancy Yes (nonreducing) Nonproliferative IgG C3 IgG1 SE, segmental deposits
Sema3B-MN (n=11) 7a; 36b 6:4 Negative Family history Yes Nonproliferative IgG, TBM + C3 IgG1 SE, TRI, TBM +
PCDH7-MN (n=10) 61 3:1 Negative None Yes Nonproliferative IgG −/Trace IgG1, IgG4 SE

The numbers in parenthesis represent the total patients with each specific type of MN that were part of the original studies. M, male; F, female; LM, light microscopy; EM, electron microscopy; ANA, anti-nuclear antibody; dsDNA, double-stranded DNA; SSA, anti–Sjögren syndrome–related antigen A; SSB, anti–Sjögren syndrome–related antigen B; MCTD, mixed connective tissue disease; SE, subepithelial; ME, mesangial; SU, subendothelial; TRI, tubuloreticular inclusions.

a

Age in children.

b

Age in young adults.