WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasia
Author:
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00467-024-06293-w.pdf
Reference5 articles.
1. Nagano C, Yamamura T, Horinouchi T, Aoto Y, Ishiko S, Sakakibara N, Shima Y, Nakanishi K, Nagase H, Iijima K, Nozu K (2020) Comprehensive genetic diagnosis of Japanese patients with severe proteinuria. Sci Rep 10:270. https://doi.org/10.1038/s41598-019-57149-5
2. Zirn B, Wittmann S, Gessler M (2005) Novel familial WT1 read-through mutation associated with Wilms tumor and slow progressive nephropathy. Am J Kidney Dis 45:1100–1104. https://doi.org/10.1053/j.ajkd.2005.03.013
3. Hughson MD, McManus JF, Hennigar GR (1978) Studies on “end-stage” kidneys. II. Embryonal hyperplasia of Bowman’s capsular epithelium. Am J Pathol 91:71–84
4. Fukuzawa R, Eccles MR, Ikeda M, Hata J (2003) Embryonal hyperplasia of Bowman’s capsular epithelium in patients with WT1 mutations. Pediatr Nephrol 18:9–13. https://doi.org/10.1007/s00467-002-1019-7
5. Sarlos DP, Banyai D, Peterfi L, Szanto A, Kovacs G (2018) Embryonal origin of metanephric adenoma and its differential diagnosis. Anticancer Res 38:6663–6667. https://doi.org/10.21873/anticanres.13033
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