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Article

Fibronectin glomerulopathy caused by genetic FN1 mutation: A case report and literature review.

Clinical nephrology - 1 May 2026

Shi Bairu, Xia Yang, Li Kejia, Jin Long, Sun Xian, Yu Hui

Abstract excerpt

BACKGROUND: Fibronectin glomerulopathy (FGP), also known as fibronectin deposition glomerulopathy (GFND), is a rare hereditary autosomal dominant glomerular disease. Its clinical manifestations are proteinuria, hematuria, hypertension, and hyperkalemic distal renal tubular acidosis, which often progresses slowly to end-stage renal disease. CASE DESCRIPTION: We report a 21-year-old woman with fibronectin...

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Identifiers

PMID: 41642109
DOI: 10.5414/CN111907

Genes

FN1

Variants

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

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