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Fig. 3 | BMC Medical Genetics

Fig. 3

From: A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report

Fig. 3

Renal pathological findings from Case II-1 at 2 weeks of age. a About half of the glomeruli showed segmental sclerosis (arrows). Hematoxylin and eosin staining, original magnification × 400. b Ultrastructurally, the glomerular basement membranes exhibit normal thickness, but show focal subendothelial widening (arrowheads). No electron-dense deposits were found. Epithelial cell foot processes show focal marked effacement (arrows). Original magnification × 5000

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