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10.1155/2018/1727986 http://scihub22266oqcxt.onion/10.1155/2018/1727986 C5872611!5872611!29732228     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Case+Rep+Nephrol 2018 ; 2018 (ä): ä Nephropedia Template TP {{tp|p=29732228|t=2018. De Novo Atypical Haemolytic Uremic Syndrome after Kidney Transplantation |pdf=|usr=}}{{29732228}} gab.com Text De Novo Atypical Haemolytic Uremic Syndrome after Kidney Transplantation JO: Case Rep Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=29732228 #FOAvip De novo thrombotic microangiopathy (TMA) can occur after kidney transplantation. An abnormality of the alternative pathway of complement must be suspected and searched for, even in presence of a secondary cause. We report the case of a 23-year-old female patient who was transplanted with a kidney from her mother for end-stage renal disease secondary to Hinman syndrome. Early after transplantation, she presented with 2 episodes of severe pyelonephritis, associated with acute kidney dysfunction and biological and histological features of TMA. Investigations of the alternative pathway of the complement system revealed atypical haemolytic uremic syndrome secondary to complement factor I mutation, associated with mutations in CD46 and complement factor H related protein genes. Plasma exchanges followed by eculizumab injections allowed improvement of kidney function without, however, normalization of creatinine. Twit Text FOAVip De Novo Atypical Haemolytic Uremic Syndrome after Kidney Transplantation ????Case Rep Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=29732228 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29732228 #FOAvip English Wikipedia <ref>{{Cite pmid|29732228}}</ref> De Novo Atypical Haemolytic Uremic Syndrome after Kidney Transplantation #MMPMID29732228 Devresse A; de Meyer M; Aydin S; Dahan K; Kanaan N Case Rep Nephrol 2018[]; 2018 (ä): ä PMID29732228show ga De novo thrombotic microangiopathy (TMA) can occur after kidney transplantation. An abnormality of the alternative pathway of complement must be suspected and searched for, even in presence of a secondary cause. We report the case of a 23-year-old female patient who was transplanted with a kidney from her mother for end-stage renal disease secondary to Hinman syndrome. Early after transplantation, she presented with 2 episodes of severe pyelonephritis, associated with acute kidney dysfunction and biological and histological features of TMA. Investigations of the alternative pathway of the complement system revealed atypical haemolytic uremic syndrome secondary to complement factor I mutation, associated with mutations in CD46 and complement factor H related protein genes. Plasma exchanges followed by eculizumab injections allowed improvement of kidney function without, however, normalization of creatinine. äDe Novo Atypical Haemolytic Uremic Syndrome after Kidney Transplantati(epmc).pdf DeepDyve Pubget Overpricing