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Article

Steroid-resistant nephrotic syndrome: impact of genetic testing.

Annals of Saudi medicine - 1 Jan 2000

Kari Jameela A, El-Desoky Sherif M, Gari Mamdooh, Malik Khalid, Vega-Warner Virginia, Lovric Svjetlana, Bockenhauer Detlef

Abstract excerpt

BACKGROUND AND OBJECTIVES: Mutations in several genes are known to cause steroid-resistant nephrotic syndome (SRNS), most commonly in NPHS1, NPHS2, and WT1. Our aims were to determine the frequency of mutations in these genes in children with SRNS, the response of patients with SRNS to various immunosuppressants, and the disease outcome, and to review the predictive value of genetic testing and renal biopsy...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 24413855
DOI: 10.5144/0256-4947.2013.533
PMCID: PMC6074900

Genes

NPHS1
NPHS2

Provenance

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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