251 top medical experts on Alkaptonuria across 41 countries and 16 U.S. states, including 69 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Alkaptonuria: An inborn error of amino acid metabolism resulting from a defect in the enzyme homogentisate 1,2-dioxygenase, an enzyme involved in the breakdown of phenylalanine and tyrosine. It is characterized by accumulation of homogentisic acid in the urine, ochronosis in various tissues, and arthritis.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Errors Amino Acid Metabolism (1,295).
  4. Clinical Trials ClinicalTrials.gov : at least 8 including 4 Completed, 2 Recruiting


  

        

                    


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