Fibronectin glomerulopathy complicated with persistent cloaca and congenital esophageal atresia: a case report and literature review

BACKGROUND: Fibronectin glomerulopathy is a rare, inherited, autosomal dominant, glomerular disease characterized by proteinuria, microscopic hematuria, hypertension, massive glomerular deposits of fibronectin, and slow progression to end-stage renal failure. Because the incident of fibronectin glom...

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Detalles Bibliográficos
Autores principales: Takii, Misaki, Suehiro, Takaichi, Shima, Aya, Yotsueda, Hideki, Hisano, Satoshi, Katafuchi, Ritsuko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588616/
https://www.ncbi.nlm.nih.gov/pubmed/28877681
http://dx.doi.org/10.1186/s12882-017-0704-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588616/
https://www.ncbi.nlm.nih.gov/pubmed/28877681
http://dx.doi.org/10.1186/s12882-017-0704-5

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