46 top medical experts on Type I 3-Methylglutaconic Aciduria across 5 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type I 3-Methylglutaconic Aciduria: 3-methylglutaconic aciduria (3-MGA) type I is an inborn error of leucine metabolism with a variable clinical phenotype ranging from mildly delayed speech to psychomotor retardation, coma, failure to thrive, metabolic acidosis and dystonia.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: 3-Methylglutaconyl-CoA Hydratase Deficiency,  3-Mg-CoA-Hydratase Deficiency,  Type I MGA


  

        

                    


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