166 top medical experts on Acute Hepatic Porphyria across 20 countries and 10 U.S. states, including 19 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Acute Hepatic Porphyria: A rare sub-group of porphyrias characterized by the occurrence of neuro-visceral attacks with or without cutaneous manifestations. Acute hepatic porphyrias encompass four diseases: acute intermittent porphyria (the most common), variagate porphyria, hereditary coproporphyria, and hereditary deficit of delta-aminolevulinic acid dehydratase (extremely rare).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: ALAD Deficiency,  Delta-Aminolevulinate Dehydratase Deficiency,  Doss Porphyria,  Porphobilinogen Synthase Deficiency


  

        

                    


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