18 top medical experts on Type IXD Glycogen Storage Disease across 2 countries and 1 U.S. states, including 2 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type IXD Glycogen Storage Disease: Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterized by exercise intolerance.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: GSD IXD,  GSD9D,  X-Linked Muscle Glycogenosis,  Muscle Phosphorylase Kinase Deficiency


  

        

                    


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