glycogen storage disease
Any of several heritable diseases characterized by the abnormal storage and accumulation of glycogen in the tissues, esp. in the liver. These diseases are grouped into various types according to the enzyme deficiency responsible.
SYN: SEE: glycogenosis
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Citation
Venes, Donald, editor. "Glycogen Storage Disease." Taber's Medical Dictionary, 25th ed., F.A. Davis Company, 2025. Nursing Central, nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/741830/all/phosphorylase_b_kinase_deficiency_glycogen_storage_disease.
Glycogen storage disease. In: Venes DD, ed. Taber's Medical Dictionary. F.A. Davis Company; 2025. https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/741830/all/phosphorylase_b_kinase_deficiency_glycogen_storage_disease. Accessed May 11, 2025.
Glycogen storage disease. (2025). In Venes, D. (Ed.), Taber's Medical Dictionary (25th ed.). F.A. Davis Company. https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/741830/all/phosphorylase_b_kinase_deficiency_glycogen_storage_disease
Glycogen Storage Disease [Internet]. In: Venes DD, editors. Taber's Medical Dictionary. F.A. Davis Company; 2025. [cited 2025 May 11]. Available from: https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/741830/all/phosphorylase_b_kinase_deficiency_glycogen_storage_disease.
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