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10.1186/s13023-015-0368-9 http://scihub22266oqcxt.onion/10.1186/s13023-015-0368-9 C4666198!4666198 !26627182     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\26627182 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Orphanet+J+Rare+Dis 2015 ; 10 (ä): 151 Nephropedia Template TP {{tp|p=26627182 |t=2015. Zellweger spectrum disorders: clinical overview and management approach |pdf=|usr=}}{{26627182 }} gab.com Text Zellweger spectrum disorders: clinical overview and management approach JO: Orphanet J Rare Dis http://www.kidney.de/pget.php?&tw=1&pmid=26627182 #FOAvip Zellweger spectrum disorders (ZSDs) represent the major subgroup within the peroxisomal biogenesis disorders caused by defects in PEX genes. The Zellweger spectrum is a clinical and biochemical continuum which can roughly be divided into three clinical phenotypes. Patients can present in the neonatal period with severe symptoms or later in life during adolescence or adulthood with only minor features. A defect of functional peroxisomes results in several metabolic abnormalities, which in most cases can be detected in blood and urine. There is currently no curative therapy, but supportive care is available. This review focuses on the management of patients with a ZSD and provides recommendations for supportive therapeutic options for all those involved in the care for ZSD patients. Twit Text FOAVip Zellweger spectrum disorders: clinical overview and management approach ????Orphanet J Rare Dis http://www.kidney.de/pget.php?&tw=1&pmid=26627182 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26627182 #FOAvip English Wikipedia <ref>{{Cite pmid|26627182 }}</ref> Zellweger spectrum disorders: clinical overview and management approach #MMPMID26627182 Klouwer FC ; Berendse K ; Ferdinandusse S ; Wanders RJ ; Engelen M ; Poll-The BT Orphanet J Rare Dis 2015[Dec]; 10 (ä): 151 PMID26627182 show ga Zellweger spectrum disorders (ZSDs) represent the major subgroup within the peroxisomal biogenesis disorders caused by defects in PEX genes. The Zellweger spectrum is a clinical and biochemical continuum which can roughly be divided into three clinical phenotypes. Patients can present in the neonatal period with severe symptoms or later in life during adolescence or adulthood with only minor features. A defect of functional peroxisomes results in several metabolic abnormalities, which in most cases can be detected in blood and urine. There is currently no curative therapy, but supportive care is available. This review focuses on the management of patients with a ZSD and provides recommendations for supportive therapeutic options for all those involved in the care for ZSD patients. |*Disease Management [MESH] |Humans [MESH] |Mutation/genetics [MESH] |Peroxisomes/genetics [MESH]Zellweger spectrum disorders: clinical overview and management approac(epmc).pdf DeepDyve Pubget Overpricing