Fig. 1From: Identification and functional characterization of the first deep intronic GLA mutation (IVS4+1326C>T) causing renal variant of Fabry diseaseA–C Kidney biopsies of the patient. A Tissue was stained with periodic acid-Schiff reagent, revealing two glomeruli with enlarged and vacuolated podocytes. Magnification, 400×. B Tissue was stained with periodic acid silver methenamine, showing one glomerulus with segmental sclerosis. Magnification, 400×. C Electron micrograph showing abundant, electron-dense myelin structures within the cytoplasm of podocytes. Magnification, 5000×Back to article page