238 top medical experts on Erythropoietic Protoporphyria across 26 countries and 19 U.S. states, including 83 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Erythropoietic Protoporphyria: An autosomal dominant porphyria that is due to a deficiency of ferrochelatase (heme synthetase) in both the liver and the bone marrow, the last enzyme in the 8-enzyme biosynthetic pathway of heme. Clinical features include mainly neurological symptoms, rarely cutaneous lesions, and elevated levels of protoporphyrin and coproporphyrins in the feces.
  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 19 including 1 Active, 13 Completed, 2 Recruiting


  

        

                    


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