200 top medical experts on Variegate Porphyria across 15 countries and 2 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. Variegate Porphyria: An autosomal dominant porphyria that is due to a deficiency of protoporphyrinogen oxidase (EC 1.3.3.4) in the liver, the seventh 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, coproporphyrins and protoporphyrinogen.
  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 5 including 1 Active, 2 Completed, 1 Recruiting
  5. Synonyms: South African Type Porphyria


  

        

                    


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