Glycogen storage disease type III
Glycogen storage disease (GSD) is an autosomal recessive genetic disease, a type of glycogen metabolism disorder caused by congenital enzyme (debranching enzyme) deficiency. Glycogen storage disease type Ⅲ is Cori type Ⅲ glycogen storage syndrome, also known as Cori disease, debranching enzyme deficiency, Forbes disease, limited dextrinosis, debranching enzyme glycogen storage disease, Forbes syndrome, etc. This disease causes the most serious liver damage.
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Site of disease:
whole body -
Infectious :
Not contagious -
Frequent population:
child -
Related symptoms:
Muscle atrophy Liver enlargement Slow growth Hepatomegaly Muscle weakness -
Concurrent disease:
Related Drugs
Children like to eat syrup
Manufacturer:
Weifang Tianyang Pharmaceutical Co., Ltd.
Related Ingredients