Glycogen Storage DiseasePresented by: Colleen Poling

What isGlycogen 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 DiseaseType II GSD

• AKA: Acid Maltase Deficiency (AMD), Pompe Disease

Therapy/Treatments for GSD type II

Type III Glycogen Storage DiseaseType III GSD

• AKA: Debrancher Deficiency, Cori Disease, Forbes Disease, Limit Dextrinosis

Therapy/Treatments for Type III GSD

Type IV Glycogen Storage DiseaseType IV GSD

• AKA: Brancher Deficiency, Andersen Disease, Amylopectinosis,Adult Polyglucosan Body Disease (APBD)

Therapy/Treatments for Type IV GSD

Type V Glycogen Storage DiseaseType V GSD

• AKA: Muscle Phosphorylase Deficiency, McArdle Disease, Myophosphorylase Deficiency 

Therapy/Treatments for Type V GSD

Type VI Glycogen Storage DiseaseType VI GSD

• AKA: Liver Phosphorylase Deficiency, Hers Disease 

Therapy/Treatments for Type VI GSD

Type VII Glycogen Storage DiseaseType VII GSD

• AKA: Muscle Phosphofructokinase Deficiency, Tarui Disease

Therapy/Treatments for Type VII GSD

Type IX Glycogen Storage DiseaseType IX GSD

• AKA: Phosphorylase Kinase Deficiency

Therapy/Treatments for Type IX GSD

Type 0 Glycogen Storage DiseaseType 0 GSD

• AKA: Hepatic Glycogen Synthase Deficiency

Therapy/Treatments for Type 0 GSD