179 top medical experts on Short chain Acyl CoA dehydrogenase deficiency across 14 countries and 6 U.S. states, including 15 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Short chain Acyl CoA dehydrogenase deficiency: Short-chain acyl-CoA dehydrogenase (SCAD) deficiency is a very rare inborn error of mitochondrial fatty acid oxidation characterized by variable manifestations ranging from asymptomatic individuals (in most cases) to those with failure to thrive, hypotonia, seizures, developmental delay and progressive myopathy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Acads Deficiency,  Deficiency Of Short-Chain Acyl-Coa Dehydrogenase,  Deficiency of Butyryl-Coa Dehydrogenase,  Lipid-Storage Myopathy Secondary to Short-Chain Acyl-Coa Dehydrogenase Deficiency,  Scad Deficiency,  Scadh Deficiency,  Short-Chain Acyl-Coa Dehydrogenase Deficiency,  Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency


  

        

                    


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