منابع مشابه
Fibronectin glomerulopathy
Fibronectin glomerulopathy occurs between the second and fifth decades of life in most patients, and it is known to be slowly progressive with mild proteinuria leading to kidney failure. The case of a 78-year-old woman with a rapid course of nephrotic syndrome due to fibronectin glomerulopathy is reported. She had proteinuria that rapidly increased to 6.8 g/day in a month and microscopic haemat...
متن کاملFibronectin Glomerulopathy: A Rare Autosomal Dominant Glomerular Disease
A 43‐year‐old female was admitted to the Department of Nephrology at Jinling Hospital (Nanjing, China) in January 2017 complaining of edema for 3 months with urine abnormalities. Her father had renal disease (with no biopsy performed) when he was 40 years old and died of uremia at 56 years old. Her mother and brother were healthy; however, her daughter and nephew (her brother’s son) had slightl...
متن کاملA Case of Fibronectin Glomerulopathy Caused by Missense Mutations in the Fibronectin 1 Gene
Shuma Hirashio, Yumi Yamada, Kouichi Mandai, Shigeo Hara and Takao Masaki Department of Nephrology, National Hospital Organization Higashihiroshima Medical Center, Hiroshima, Japan; Department of Nephrology, Hiroshima University Hospital, Hiroshima, Japan; Department of Diagnostic Pathology, National Hospital Organization Higashihiroshima Medical Center, Hiroshima, Japan; and Department of Diag...
متن کاملFibronectin glomerulopathy: an uncommon cause of nephrotic syndrome in systemic lupus erythematosus
A renal biopsy in a case of systemic lupus erythematosus (SLE) nephritis presenting with both nephrotic syndrome (NS) and acute renal failure (ARF) demonstrated atypical fibrillary deposits in the glomerular mesangium and subendothelium. The size and morphology of fibrils resembled those of fibronectin (FN) glomerulopathy [1,2], as also confirmed by immunoperoxidase staining. As no familial his...
متن کاملFibronectin 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 glomerulopathy is extremely low, the pathophysiology, genetic abnormalities, epidemiology, and mechani...
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ژورنال
عنوان ژورنال: Clinical Kidney Journal
سال: 2013
ISSN: 2048-8505,2048-8513
DOI: 10.1093/ckj/sft097