171 top medical experts on HHH syndrome across 20 countries and 1 U.S. states, including 17 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. HHH syndrome: A rare, genetic disorder of urea cycle metabolism characterized by either a neonatal-onset with manifestations of lethargy, poor feeding, vomiting and tachypnea or, more commonly, presentations in infancy, childhood or adulthood with chronic neurocognitive deficits, acute encephalopathy and/or coagulation defects or other chronic liver dysfunction.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Hyperornithinemia-Hyperammonemia-Homocitrullinemia Syndrome,  Hyperornithinemia-hyperammonemia-homocitrullinuria,  Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome,  Ornithine translocase deficiency,  Triple H Syndrome


  

        

                    


    Computing Expert Listing ...