Recent Blog Posts

View Post: all babies in england to be screened for medium chain acyl coa ...
14 Sep 2009 by latermmegi  
all babies in england are to be screened for the purpose an inherited metabolic affliction called technique check acyl coa dehydrogenase deficiency (mcadd), within two weeks of delivery, announced health vicar, ivan lewis today. ...
View Blog: latermmegi - http://latermmegi.queeredin.com/

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View Post: Neonatal Screening for Very Long-Chain Acyl-CoA Dehydrogenase ...
1 Sep 2006 by Liebig, M., Schymik, I., Mueller, M., Wendel,...  
Abbreviations: VLCADD—very long-chain acyl-coenzyme A dehydrogenase deficiency • MS/MS—tandem mass spectrometry • CoA—coenzyme A • MCADD—medium-chain acyl-coenzyme A dehydrogenase deficiency ...
View Blog: PEDIATRICS recent issues - http://pediatrics.aappublications.org/

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View Post: Carnitine Palmitoyltransferase II Deficiency Clinical Trial ...
22 Sep 2009
Djouadi et al. established that administration to control mice of a CPT I inhibitor (etomoxir) causes a feedback induction of PPARα target genes involved in fatty acid oxidation such as medium-chain acyl-CoA dehydrogenase and acyl-CoA ...
View Blog: Clinical Trials Updates During the Last 7 Days - http://clinicaltrialsfeeds.org/clinical-trials/r...

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View Post: 76 Pediatric Deaths Due to H1N1- Special Precautions for Children ...
12 Oct 2009 by Dr. Desiree Jones  
Finally, children with poor nutritional and fluid intake because of prolonged vomiting and diarrhea, and children with an underlying metabolic disorder such as Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency – are more susceptible ...
View Blog: The Prevention Revolution - http://thepreventionrevolution.com/

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View Post: Metabolic acidosis. Hyperammonemia
14 Oct 2009 by Disorders  
If there are no ketones present then you may have a defect in fatty acid oxidation, such as MCAD, medium chain acyl-CoA dehydrogenase deficiency, which is not as uncommon as we used to think. So this is just a general algorithm that ...
View Blog: Diseases, Disorders information - http://www.disordersinformation.com/

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View Post: Birmingham Children's Hospital completes development of laboratory ...
17 Sep 2009
... recommends that all babies in the UK are offered screening for phenylketonuria (PKU), congenital hypothyroidism (CHT), sickle cell disorders (SCD), cystic fibrosis (CF) and medium-chain acyl-CoA dehydrogenase deficiency (MCADD). ...
View Blog: The British Journal of Healthcare Computing... - http://www.bjhcim.co.uk/

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