27 top medical experts on Dicarboxylicaminoaciduria across 4 countries, including 3 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Dicarboxylicaminoaciduria: Dicarboxylicaminoaciduria is characterised by infantile-onset hypoglycaemia and hyperprolinaemia associated, in certain cases, with intellectual deficit.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Dicarboxylic amino aciduria,  Dicarboxylic aminoaciduria,  Dicarboxylicamino Aciduria,  Glutamate and aspartate transport defect,  Glutamate-Aspartate Transport Defect,  Inborn error of glutamic and aspartate transport


  

        

                    


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