53 top medical experts on Hyperlysinemias across 3 countries and 2 U.S. states, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hyperlysinemias: A group of inherited metabolic disorders which have in common elevations of serum lysine levels. Enzyme deficiencies of alpha-aminoadipic semialdehyde dehydrogenase and the saccharopine dehydrogenases have been associated with hyperlysinemia. Clinical manifestations include mental retardation, recurrent emesis, hypotonia, lethargy, diarrhea, and developmental delay. (From Menkes, Textbook of Child Neurology, 5th ed, p56)
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Errors Amino Acid Metabolism (1,295), Inborn Metabolic Brain Diseases (1,358).
  4. Synonyms: Alpha-Aminoadipic Semialdehyde Deficiency Disease,  Lysine Alpha-Ketoglutarate Reductase Deficiency Disease,  Saccharopine Dehydrogenase Deficiency Disease


  

        

                    


    Computing Expert Listing ...

);