5 top medical experts on Dimethylglycine Dehydrogenase Deficiency across 0 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Dimethylglycine Dehydrogenase Deficiency: Dimethylglycine dehydrogenase deficiency is an extremely rare autosomal recessive glycine metabolism disorder characterized clinically in the single reported case to date by muscle fatigue and a fish-like odor.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: DMGDH Deficiency,  DMGDHD


  

        

                    


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