33 top medical experts on Glycogen Storage Disease XII across 5 countries and 1 U.S. states. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Glycogen Storage Disease XII: Glycogen storage disease due to aldolase A deficiency is an extremely rare glycogen storage disease (see this term) characterized by hemolytic anemia with or without myopathy or intellectual deficit. Myopathy can be severe enough to result in fatal rhabdomyolysis in some patients. A family with episodic rhabdomyolysis (triggered by fever) without hemolytic anemia has recently been reported.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: ALDOA Deficiency,  Aldolase A Deficiency,  Red Cell Aldolase Deficiency,  GSD XII,  GSD12,  Red Cell Aldolase Deficiency


  

        

                    


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