Article

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

2026-01-22

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<title>Abstract</title> <p>Objective This study characterizes a pediatric case of glomerulopathy with fibronectin deposits (GFND) caused by a novel FN1 variant and investigates the evidence for systemic involvement and genotype-phenotype correlations through a comprehensive literature review. Methods We report a female child diagnosed with GFND in February 2017 based on renal biopsy and genetic testing at our i...

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Literature Corpus work: 48f18d37-b80d-5d7e-b473-991c2ac84f93
DOI: 10.21203/rs.3.rs-8633975/v1

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