Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A child with genetic FN1 mutation in the absence of classic glomerulopathy with fibronectin deposits(GFND) findings on biopsy.

BMC nephrology - 14 Jul 2022

Yang Xiao-Qing, Shen Tong

Abstract excerpt

BACKGROUND: Glomerulopathy with fibronectin deposits (GFND) is a rare autosomal dominant genetic disorder, and proteinuria and hematuria are the most common clinical manifestations. The pathogenesis of this disease is primarily related to mutation of the fibronectin 1 gene. Unfortunately, without specific treatment, the prognosis remains poor. Here we present a case report that investigates the clinical...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Biopsy
Share to Fibronectins
Share to Glomerulonephritis, Membranoproliferative

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hematuria

Share to Kidney Failure, Chronic

Share to Nephritis, Hereditary

Share to Proteinuria

Share to Renal Insufficiency

Source

Open in PubMed Open full text

Identifiers

PMID: 35836154
DOI: 10.1186/s12882-022-02872-x
PMCID: PMC9284822

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A child with genetic FN1 mutation in the absence of classic glomerulopathy with fibronectin deposits(GFND) findings on biopsy.PMID 35836154Read ↗

A novel variant in FN1 in a family with fibronectin glomerulopathySemantic proximity Read ↗

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 ↗

Rapidly Progressive Pediatric Fibronectin Glomerulopathy Driven by a Novel FN1 Mutation (p.Thr1917del): Implications for Early Diagnosis and Recognition of Systemic InvolvementSemantic proximity Read ↗

Aberrant serum-derived FN1 variants bind to integrin β1 on glomerular endothelial cells contributing to thin basement membrane nephropathy.Semantic proximity Read ↗

Fibronectin Glomerulopathy: A Case Report of Membranoproliferative Glomerulonephritis.Semantic proximity Read ↗

A Case of Unexpected Diagnosis of Fibronectin Glomerulopathy with Histological Features of Membranoproliferative GlomerulonephritisSemantic proximity Read ↗

[Glomerulopathy with fibronectin deposits caused by FN1 gene mutation: A familial case report and literature review].Semantic proximity Read ↗

Fibronectin glomerulopathy caused by genetic FN1 mutation: A case report and literature review.Semantic proximity Read ↗

Phenotype-Genotype Correlations in Three Different Cases of Adult-Onset Genetic Focal Segmental Glomerulosclerosis.Semantic proximity Read ↗

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.Semantic proximity Read ↗

Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.Semantic proximity Read ↗

Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.