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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Identification and functional characterization of the first deep intronic GLA mutation (IVS4+1326C>T) causing renal variant of Fabry disease

Fig. 1

A–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×

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