211 top medical experts on Erythropoietic Porphyria across 19 countries and 10 U.S. states, including 48 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Erythropoietic Porphyria: An autosomal recessive porphyria that is due to a deficiency of uroporphyrinogen III synthase in the bone marrow; also known as congenital erythropoietic porphyria. This disease is characterized by splenomegaly; anemia; photosensitivity; cutaneous lesions; accumulation of hydroxymethylbilane; and increased excretion of uroporphyrins 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): Genetic Skin Diseases (3,548), Porphyrias (556).
  4. Clinical Trials ClinicalTrials.gov : at least 36 including 5 Active, 22 Completed, 4 Recruiting
  5. Synonyms: Deficiency of Uroporphyrinogen III Synthase,  Gunther's Disease,  Congenital Erythropoietic Porphyria,  Deficiency of Uroporphyrinogen III Synthase


  

        

                    


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