203 top medical experts on Glycogen Storage Disease Type IV across 16 countries and 10 U.S. states, including 38 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Glycogen Storage Disease Type IV: An autosomal recessive metabolic disorder due to a deficiency in expression of glycogen branching enzyme 1 (alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accumulation of abnormal glycogen with long outer branches. Clinical features are muscle hypotonia and cirrhosis. Death from liver disease usually occurs before age 2.
  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 4 including 1 Active, 1 Completed, 1 Recruiting
  5. Synonyms: Amylopectinosis,  Andersen Disease,  Brancher Deficiency,  Glycogenosis 4


  

        

                    


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