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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Detaylı Bibliyografya
Yayımlandı:BMC Nephrol
Asıl Yazarlar: Takii, Misaki, Suehiro, Takaichi, Shima, Aya, Yotsueda, Hideki, Hisano, Satoshi, Katafuchi, Ritsuko
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2017
Konular:
Case Report
Online Erişim: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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