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10.4132/jptm.2015.08.31 http://scihub22266oqcxt.onion/10.4132/jptm.2015.08.31 C4804144!4804144!26755355     free     free     free Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Pathol+Transl+Med 2016 ; 50 (2): 160-4 Nephropedia Template TP {{tp|p=26755355|t=2016. An Adult Case of Bartter Syndrome Type III Presenting with Proteinuria |pdf=|usr=}}{{26755355}} gab.com Text An Adult Case of Bartter Syndrome Type III Presenting with Proteinuria JO: J Pathol Transl Med http://www.kidney.de/pget.php?&tw=1&pmid=26755355 #FOAvip Bartter syndrome (BS) I?IV is a rare autosomal recessive disorder affecting salt reabsorption in the thick ascending limb of the loop of Henle. This report highlights clinicopathological findings and genetic studies of classic BS in a 22-year-old female patient who presented with persistent mild proteinuria for 2 years. A renal biopsy demonstrated a mild to moderate increase in the mesangial cells and matrix of most glomeruli, along with marked juxtaglomerular cell hyperplasia. These findings suggested BS associated with mild IgA nephropathy. Focal tubular atrophy, interstitial fibrosis, and lymphocytic infiltration were also observed. A genetic study of the patient and her parents revealed a mutation of the CLCNKB genes. The patient was diagnosed with BS, type III. This case represents an atypical presentation of classic BS in an adult patient. Pathologic findings of renal biopsy combined with genetic analysis and clinicolaboratory findings are important in making an accurate diagnosis. Twit Text FOAVip An Adult Case of Bartter Syndrome Type III Presenting with Proteinuria ????J Pathol Transl Med http://www.kidney.de/pget.php?&tw=1&pmid=26755355 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26755355 #FOAvip English Wikipedia <ref>{{Cite pmid|26755355}}</ref> An Adult Case of Bartter Syndrome Type III Presenting with Proteinuria #MMPMID26755355 Cha EJ; Hwang WM; Yun SR; Park MH J Pathol Transl Med 2016[Mar]; 50 (2): 160-4 PMID26755355show ga Bartter syndrome (BS) I?IV is a rare autosomal recessive disorder affecting salt reabsorption in the thick ascending limb of the loop of Henle. This report highlights clinicopathological findings and genetic studies of classic BS in a 22-year-old female patient who presented with persistent mild proteinuria for 2 years. A renal biopsy demonstrated a mild to moderate increase in the mesangial cells and matrix of most glomeruli, along with marked juxtaglomerular cell hyperplasia. These findings suggested BS associated with mild IgA nephropathy. Focal tubular atrophy, interstitial fibrosis, and lymphocytic infiltration were also observed. A genetic study of the patient and her parents revealed a mutation of the CLCNKB genes. The patient was diagnosed with BS, type III. This case represents an atypical presentation of classic BS in an adult patient. Pathologic findings of renal biopsy combined with genetic analysis and clinicolaboratory findings are important in making an accurate diagnosis. äAn Adult Case of Bartter Syndrome Type III Presenting with Proteinuria(epmc).pdf DeepDyve Pubget Overpricing