Glycogen Storage Disease Presented by Colleen Poling What

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

Therapy/Treatments for GSD type II

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

Therapy/Treatments for Type III GSD

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

Therapy/Treatments for Type IV GSD

Type V Glycogen Storage Disease Type V GSD • AKA: Muscle Phosphorylase Deficiency, Mc. Ardle Disease, Myophosphorylase Deficiency

Therapy/Treatments for Type V GSD

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

Therapy/Treatments for Type VI GSD

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

Therapy/Treatments for Type VII GSD

Type IX Glycogen Storage Disease Type IX GSD • AKA: Phosphorylase Kinase Deficiency

Therapy/Treatments for Type IX GSD

Type 0 Glycogen Storage Disease Type 0 GSD • AKA: Hepatic Glycogen Synthase Deficiency

Therapy/Treatments for Type 0 GSD