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10.1016/j.ymgmr.2015.03.003 http://scihub22266oqcxt.onion/10.1016/j.ymgmr.2015.03.003 C4750558!4750558!26937394     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 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       Mol+Genet+Metab+Rep 2015 ; 3 (ä): 39-41 Nephropedia Template TP {{tp|p=26937394|t=2015. Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency |pdf=|usr=}}{{26937394}} gab.com Text Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency JO: Mol Genet Metab Rep http://www.kidney.de/pget.php?&tw=1&pmid=26937394 #FOAvip Very long chain acyl CoA dehydrogenase deficiency (VLCADD) is an inborn error in long chain fatty acid oxidation with significant variability in the severity and timing of its clinical presentation. Neonatal presentations of VLCADD have included hypoglycemia and cardiomyopathy while rhabdomyolysis is usually a later onset complication. We describe a neonate with VLCADD presenting with rhabdomyolysis prior to the return of an abnormal newborn screen. This report suggests that evaluating for rhabdomyolysis, in addition to a cardiac and hepatic work-up, is an important part of the initial evaluation of an infant with an abnormal newborn screen suggesting a diagnosis of VLCADD. Twit Text FOAVip Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency ????Mol Genet Metab Rep http://www.kidney.de/pget.php?&tw=1&pmid=26937394 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26937394 #FOAvip English Wikipedia <ref>{{Cite pmid|26937394}}</ref> Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency #MMPMID26937394 Scott Schwoerer J; Cooper G; van Calcar S Mol Genet Metab Rep 2015[Jun]; 3 (ä): 39-41 PMID26937394show ga Very long chain acyl CoA dehydrogenase deficiency (VLCADD) is an inborn error in long chain fatty acid oxidation with significant variability in the severity and timing of its clinical presentation. Neonatal presentations of VLCADD have included hypoglycemia and cardiomyopathy while rhabdomyolysis is usually a later onset complication. We describe a neonate with VLCADD presenting with rhabdomyolysis prior to the return of an abnormal newborn screen. This report suggests that evaluating for rhabdomyolysis, in addition to a cardiac and hepatic work-up, is an important part of the initial evaluation of an infant with an abnormal newborn screen suggesting a diagnosis of VLCADD. äRhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogen(epmc).pdf DeepDyve Pubget Overpricing