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Glycogen Storage Disease

Glycogen Storage Disease. Presented by: Colleen Poling. What is Glycogen Storage Disease?. Type I Glycogen Storage Disease- Type I GSD. AKA: von Gierkes disease, Type I Glycogenosis, Hepatorenal Glycogenosis . Therapy/Treatments for Type I GSD. Type II Glycogen Storage Disease Type II GSD.

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Glycogen Storage Disease

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  1. Glycogen Storage Disease Presented by: Colleen Poling

  2. What isGlycogen Storage Disease?

  3. Type I Glycogen Storage Disease-Type I GSD • AKA: von Gierkes disease, Type I Glycogenosis, Hepatorenal Glycogenosis

  4. Therapy/Treatments for Type I GSD

  5. Type II Glycogen Storage DiseaseType II GSD • AKA: Acid Maltase Deficiency (AMD), Pompe Disease

  6. Therapy/Treatments for GSD type II

  7. Type III Glycogen Storage DiseaseType III GSD • AKA: Debrancher Deficiency, Cori Disease, Forbes Disease, Limit Dextrinosis

  8. Therapy/Treatments for Type III GSD

  9. Type IV Glycogen Storage DiseaseType IV GSD • AKA: Brancher Deficiency, Andersen Disease, Amylopectinosis,Adult Polyglucosan Body Disease (APBD)

  10. Therapy/Treatments for Type IV GSD

  11. Type V Glycogen Storage DiseaseType V GSD • AKA: Muscle Phosphorylase Deficiency, McArdle Disease, Myophosphorylase Deficiency

  12. Therapy/Treatments for Type V GSD

  13. Type VI Glycogen Storage DiseaseType VI GSD • AKA: Liver Phosphorylase Deficiency, Hers Disease

  14. Therapy/Treatments for Type VI GSD

  15. Type VII Glycogen Storage DiseaseType VII GSD • AKA: Muscle Phosphofructokinase Deficiency, Tarui Disease

  16. Therapy/Treatments for Type VII GSD

  17. Type IX Glycogen Storage DiseaseType IX GSD • AKA: Phosphorylase Kinase Deficiency

  18. Therapy/Treatments for Type IX GSD

  19. Type 0 Glycogen Storage DiseaseType 0 GSD • AKA: Hepatic Glycogen Synthase Deficiency

  20. Therapy/Treatments for Type 0 GSD

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