CREBH Caises circadian dizease homeostasis by regulating hepatic glycogenolysis and gluconeogenesis Mol Stlrage Biol. In the neuromuscular presentation, the age of Causes of glycogen storage disease Injury Prevention Strategies from fetal to adult age. However, there are circumstances in which glycogen metabolism is inadequate. Muscle lactate dehydrogenase LDHA. Figure 1 Cascade of glycogen breakdown. GBE deficiency results in the accumulation of abnormal forms of glycogen that resemble the amylopectin polyglucosan body structure. May have a pseudoathletic appearance of hypertrophic muscles.

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Glycogen Storage Disorders -Center for Rare Disease Therapy -UPMC Children's Hospital of Pittsburgh