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

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 sp...

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Detalles Bibliográficos
Autores principales: Yang, Xiao-qing, Shen, Tong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284822/
https://www.ncbi.nlm.nih.gov/pubmed/35836154
http://dx.doi.org/10.1186/s12882-022-02872-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284822/
https://www.ncbi.nlm.nih.gov/pubmed/35836154
http://dx.doi.org/10.1186/s12882-022-02872-x

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