67 top medical experts on Succinyl-CoA:3-oxoacid CoA transferase deficiency across 8 countries, including 2 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Succinyl-CoA:3-oxoacid CoA transferase deficiency: A rare, genetic disorder in ketone body utilization characterized by severe, potentially fatal intermittent episodes of ketoacidosis.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: 3-Oxoacid Coa Transferase Deficiency,  Ketoacidosis due to SCOT deficiency,  SCOT deficiency,  Succinyl-Coa 3-Oxoacid Transferase Deficiency,  Succinyl-Coa:3-Ketoacid Coa Transferase Deficiency,  Succinyl-Coa:3-Ketoacid Coa-Transferase Deficiency,  Succinyl-Coa:Acetoacetate Transferase Deficiency


  

        

                    


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