Glycogen storage disease(肝醣儲積症)

症狀/併發症(symptom/complication)
病因(etiology)	|defects in degradation of glycogen |most are autosomal recessive type |參見：肝醣儲積症(Glycogen storage disease) Key to scheme: UDP-glucose, uridine diphosphoglucose; 1. hexokinase/glucokinase; 2. glucose 6-phosphatase; 3. phosphoglucomutase; 4. glycogen synthase; 5. branching enzyme; 6. glycogen phosphorylase; 7. debranching enzyme; 8. phosphofructokinase; 9. fructose 1,6-bisphosphatase; 10. acid maltase; 11. pyruvate dehydrogenase. 資料來源：英國醫學雜誌
檢查/準則(examination/criteria)
治療(treatment)
鑑別診斷(Differential Diagnosis)
流行病學(Epidemiology)

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