Among the 77 biopsies of FGN, 4 cases presented an additional concurrent disease, represented by extra-capillary glomerulonephritis ANCA-related with acute tubular necrosis (2 cases), light-chain tubulopathy without crystal formation (1 case), and thrombospondin type I domain-containing 7A (THSD7A)-positive membranous glomerulonephritis (1 case) (Table 3). The gene discussed is THSD7A; the disease is membranous glomerulonephritis.