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10.1159/000468517 http://scihub22266oqcxt.onion/10.1159/000468517 C5425770!5425770 !28503551     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28503551 &cmd=llinks): Failed to open stream: HTTP request failed! 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A Case of Fibrillary Glomerulonephritis with Fibril Deposition in the Arteriolar Wall and a Family History of Renal Disease |pdf=|usr=}}{{28503551 }} gab.com Text A Case of Fibrillary Glomerulonephritis with Fibril Deposition in the Arteriolar Wall and a Family History of Renal Disease JO: Case Rep Nephrol Dial http://www.kidney.de/pget.php?&tw=1&pmid=28503551 #FOAvip Herein, we report a case of fibrillary glomerulonephritis (FGN). FGN usually shows non-amyloidal fibrils in the mesangium and glomerular capillary walls on electron microscopy. Inherited cases of FGN have been reported in only 3 families, and the suspected genetic form was autosomal dominant. In the present case, the deposition of microfibrils in the arteriolar wall as well as the glomerulus is unique. Our patient's father died of nephrotic syndrome, and his elder brother had a biopsy-proven glomerulopathy. The histological findings of the brothers are similar to mesangial proliferative glomerulonephritis and resemble each other. Therefore, our case is presumed to be familial FGN. Additionally, herein, we review the literature and reconsider the histological and clinical characters of FGN. Twit Text FOAVip A Case of Fibrillary Glomerulonephritis with Fibril Deposition in the Arteriolar Wall and a Family History of Renal Disease ????Case Rep Nephrol Dial http://www.kidney.de/pget.php?&tw=1&pmid=28503551 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28503551 #FOAvip English Wikipedia <ref>{{Cite pmid|28503551 }}</ref> A Case of Fibrillary Glomerulonephritis with Fibril Deposition in the Arteriolar Wall and a Family History of Renal Disease #MMPMID28503551 Watanabe K ; Nakai K ; Hosokawa N ; Watanabe S ; Kono K ; Goto S ; Fujii H ; Hara S ; Nishi S Case Rep Nephrol Dial 2017[Jan]; ä (1 ): 26-33 PMID28503551 show ga Herein, we report a case of fibrillary glomerulonephritis (FGN). FGN usually shows non-amyloidal fibrils in the mesangium and glomerular capillary walls on electron microscopy. Inherited cases of FGN have been reported in only 3 families, and the suspected genetic form was autosomal dominant. In the present case, the deposition of microfibrils in the arteriolar wall as well as the glomerulus is unique. Our patient's father died of nephrotic syndrome, and his elder brother had a biopsy-proven glomerulopathy. The histological findings of the brothers are similar to mesangial proliferative glomerulonephritis and resemble each other. Therefore, our case is presumed to be familial FGN. Additionally, herein, we review the literature and reconsider the histological and clinical characters of FGN. äA Case of Fibrillary Glomerulonephritis with Fibril Deposition in the (epmc).pdf DeepDyve Pubget Overpricing