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10.4103/sja.SJA_699_17 http://scihub22266oqcxt.onion/10.4103/sja.SJA_699_17 C5875229!5875229!29628851     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       Saudi+J+Anaesth 2018 ; 12 (2): 332-4 Nephropedia Template TP {{tp|p=29628851|t=2018. Renal oxalate stones in children with Zellweger spectrum disorders |pdf=|usr=}}{{29628851}} gab.com Text Renal oxalate stones in children with Zellweger spectrum disorders JO: Saudi J Anaesth http://www.kidney.de/pget.php?&tw=1&pmid=29628851 #FOAvip Peroxisomal biogenesis disorders due to PEX gene defects are classified into many subgroups, of which Zellweger spectrum disorders (ZSDs) represent the major subgroup. The ZSDs are clinical and biochemical disorders divided into three phenotypes: neonatal, adolescence, or adult. Clinical presentations vary with severity of the condition. Metabolic abnormalities occur due to functional peroxisomal defects that could be detected in blood and urine. No cure or definitive management exists to date; only supportive and palliative measures are applied to prevent worse sequelae. We experienced a case of oxalate renal stones in a patient with ZSD. This patient had hyperoxaluria and hyperglycolic aciduria with clinically associated clues that correlate with urinary oxalate load. Urinary oxalate and glycolate excretion were assessed. Radiological workup revealed renal involvement with urolithiasis and nephrocalcinosis. Urinalysis and ultrasonography for stones and hyperoxaluria should be used to screen patients with ZSD for early intervention to prevent renal damage. Twit Text FOAVip Renal oxalate stones in children with Zellweger spectrum disorders ????Saudi J Anaesth http://www.kidney.de/pget.php?&tw=1&pmid=29628851 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29628851 #FOAvip English Wikipedia <ref>{{Cite pmid|29628851}}</ref> Renal oxalate stones in children with Zellweger spectrum disorders #MMPMID29628851 Alhazmi HH Saudi J Anaesth 2018[Apr]; 12 (2): 332-4 PMID29628851show ga Peroxisomal biogenesis disorders due to PEX gene defects are classified into many subgroups, of which Zellweger spectrum disorders (ZSDs) represent the major subgroup. The ZSDs are clinical and biochemical disorders divided into three phenotypes: neonatal, adolescence, or adult. Clinical presentations vary with severity of the condition. Metabolic abnormalities occur due to functional peroxisomal defects that could be detected in blood and urine. No cure or definitive management exists to date; only supportive and palliative measures are applied to prevent worse sequelae. We experienced a case of oxalate renal stones in a patient with ZSD. This patient had hyperoxaluria and hyperglycolic aciduria with clinically associated clues that correlate with urinary oxalate load. Urinary oxalate and glycolate excretion were assessed. Radiological workup revealed renal involvement with urolithiasis and nephrocalcinosis. Urinalysis and ultrasonography for stones and hyperoxaluria should be used to screen patients with ZSD for early intervention to prevent renal damage. äRenal oxalate stones in children with Zellweger spectrum disorders (epmc).pdf DeepDyve Pubget Overpricing