161 top medical experts on 3-methylcrotonyl CoA carboxylase 1 deficiency across 11 countries and 6 U.S. states, including 12 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 3-methylcrotonyl CoA carboxylase 1 deficiency: A rare inherited disorder of leucine metabolism characterized by a highly variable clinical picture ranging from metabolic crisis in infancy to asymptomatic adults.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: 3 Methylcrotonyl-CoA carboxylase deficiency,  3 Methylcrotonylglycinuria,  3 alpha methylcrotonylglycinuria 1,  3-Mcc Deficiency,  3-Methylcrotonyl-Coa Carboxylase Deficiency,  3-Methylcrotonyl-Coenzyme A Carboxylase Deficiency,  3-Methylcrotonylglycinuria,  3-Methylcrotonylglycinuria I,  Bmcc Deficiency,  Deficiency of Methylcrotonoyl-Coa Carboxylase,  MCC1 Deficiency,  MCCD Type 1,  Mcc Deficiency,  Methylcrotonyl-Coa Carboxylase Deficiency,  Methylcrotonylglycinuria Type I,  methylcrotonoyl-CoA carboxylase 1 deficiency


  

        

                    


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