TY - JOUR AU - Takii, Misaki AU - Suehiro, Takaichi AU - Shima, Aya AU - Yotsueda, Hideki AU - Hisano, Satoshi AU - Katafuchi, Ritsuko PY - 2017 DA - 2017/09/06 TI - Fibronectin glomerulopathy complicated with persistent cloaca and congenital esophageal atresia: a case report and literature review JO - BMC Nephrology SP - 288 VL - 18 IS - 1 AB - 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 glomerulopathy is extremely low, the pathophysiology, genetic abnormalities, epidemiology, and mechanisms remain to be elucidated. SN - 1471-2369 UR - https://doi.org/10.1186/s12882-017-0704-5 DO - 10.1186/s12882-017-0704-5 ID - Takii2017 ER -