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

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

Abstract 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 fibronec...

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Bibliographic Details
Main Authors: Misaki Takii, Takaichi Suehiro, Aya Shima, Hideki Yotsueda, Satoshi Hisano, Ritsuko Katafuchi
Format: Article
Language:English
Published: BMC 2017-09-01
Series:BMC Nephrology
Subjects:
Fibronectin glomerulopathy
Fibronectin 1 gene
Congenital esophageal atresia
Persistent cloaca
Online Access:http://link.springer.com/article/10.1186/s12882-017-0704-5

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http://link.springer.com/article/10.1186/s12882-017-0704-5

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