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Article

A case report of congenital nephrotic syndrome caused by new mutations of NPHS1.

The Journal of international medical research - 1 Aug 2021

Li Zhong, Zhuang Lanchun, Han Mei, Li Feng

Abstract excerpt

Congenital nephrotic syndrome (CNS) is a rare autosomal recessive disorder that occurs in the first 0 to 3 months of life. The course of CNS is progressive, often leading to end-stage renal disease within 2 to 3 years. Most patients with CNS are resistant to glucocorticoids and immunosuppressive drugs. We report a girl aged 1 month and 20 days who was admitted to hospital with a history of abdominal distension...

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Identifiers

PMID: 34396835
DOI: 10.1177/03000605211038133
PMCID: PMC8371728

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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