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Fibronectin Glomerulopathy: A Case Report of Membranoproliferative Glomerulonephritis.

Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia - 30 Apr 2026

Sannino Anna, d'Angiò Pierluigi, Laurino Simona, Marino Antonella, Sellitti Maria Luigia, Urcioli Valentina, Genovese Armando, Gigliotti Giuseppe

Abstract excerpt

Background. Fibronectin glomerulopathy (FNG) is a rare autosomal dominant glomerulopathy characterized by proteinuria, hematuria, hypertension, and gradual progression to end-stage renal disease (ESRD) over 15-20 years. The disease is caused by mutations in the FN1 gene. Currently, there is no specific treatment for FNG. Case Report. A 22-year-old female presented with sub-nephrotic proteinuria and microscopic...

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Identifiers

PMID: 42143752
DOI: 10.69097/43-02-2026-09

Genes

FN1
ACE

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Fibronectin Glomerulopathy: A Case Report of Membranoproliferative Glomerulonephritis.PMID 42143752Read ↗

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Rapidly progressive pediatric fibronectin glomerulopathy driven by a novel FN1 mutation (p.Thr1917del): implications for early diagnosis and recognition of systemic involvement.Semantic proximity Read ↗

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