120 top medical experts on Hereditary Coproporphyria across 8 countries and 3 U.S. states, including 12 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hereditary Coproporphyria: An autosomal dominant porphyria that is due to a deficiency of coproporphyrinogen oxidase in the liver, the sixth enzyme in the 8-enzyme biosynthetic pathway of heme. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, 5-aminolevulinate and coproporphyrins.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hepatic Porphyrias (226).
  4. Clinical Trials ClinicalTrials.gov : at least 12 including 1 Active, 5 Completed, 3 Recruiting


  

        

                    


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