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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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| Publicado no: | BMC Nephrol |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5588616/ https://ncbi.nlm.nih.gov/pubmed/28877681 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-017-0704-5 |
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