232 top medical experts on Glutaric Acidemia I across 40 countries and 17 U.S. states, including 63 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Glutaric Acidemia I: Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Glutaric Acidemia Type 1,  Glutaric Acidemia Type I,  Glutaric Aciduria I,  Glutaric acidemia 1,  Glutaric aciduria 1,  Glutaryl-CoA dehydrogenase deficiency


  

        

                    


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