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Article

[A case of severe congenital nephrotic syndrome secondary to NPHS1 mutation].

Revue medicale de Liege - 1 Jul 2020

Quiros A, Lefèbvre C, Collard L, Rigo V, Lombet J

Abstract excerpt

The congenital nephrotic syndrome is a rare and severe pathology, and its management represents a real challenge for pediatric nephrologists. We report the case of a congenital nephrotic syndrome secondary to a homozygous mutation of the NPHS1. The young patient has a severe clinical course, and benefits of a management by anti-proteinuric treatment and a unilateral nephrectomy. This clinical case illustrates the...

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PMID: 32779909

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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