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Article

Nephrotic syndrome and end-stage renal disease with WT1 mutation detected at 3 years.

Pediatric nephrology (Berlin, Germany) - 1 Nov 1999

Ito S, Ikeda M, Takata A, Kikuchi H, Hata J, Honda M

Abstract excerpt

We report a boy who presented at 3 years with nephrotic syndrome and end-stage renal failure. Although histopathological findings showed end-stage kidney, isolated diffuse mesangial sclerosis (IDMS) was suspected because of his clinical course, and was confirmed by the presence of WT1 (Wilms tumor suppressor gene) mutation. He did not have ambiguous genitalia or Wilms tumor. The karyotype was 46:XY. A...

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Identifiers

PMID: 10603123
DOI: 10.1007/s004670050702

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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