275 top medical experts on Glycogen Storage Disease Type I across 29 countries and 22 U.S. states, including 110 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Glycogen Storage Disease Type I: An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Glycogen Storage Disease (1,538).
  4. Clinical Trials ClinicalTrials.gov : at least 11 including 1 Active, 5 Completed, 1 Recruiting
  5. Synonyms: Glucose-6-Phosphatase Deficiency,  Glucosephosphatase Deficiency,  Glycogenosis 1,  Hepatorenal Glycogen Storage Disease,  von Gierke Disease


  

        

                    


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