37 top medical experts on Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency across 4 countries, including 4 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency: Vitamin B12-unresponsive methylmalonic acidemia type mut0 is an inborn error of metabolism characterized by recurrent ketoacidotic comas or transient vomiting, dehydration, hypotonia and intellectual deficit, which does not respond to administration of vitamin B12.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: MMA due to MCM Deficiency,  Methylmalonic Acidemia due to Methylmalonyl-CoA Mutase Deficiency,  MUT Type Methylmalonic Aciduria,  mut(-) Type Methylmalonic Aciduria,  mut(0) Type Methylmalonic Aciduria


  

        

                    


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