Table 1.
Features of the Classical Glycogen Storage Diseases
Type/Eponym | Enzyme Deficiency | Presenting Clinical Features | Primary Tissue Involvement | Animal Model | Vector Administered |
---|---|---|---|---|---|
I/von Gierke | Glucose-6-phosphatase | Growth retardation, hepatomegaly, hypoglycemia, lactic acidemia, hyperuricemia, and hyperlipidemia | Liver, kidney | Maltese dog, mouse | AAV, Ad, LV, plasmid |
II/Pompe | Acid alpha-glucosidase | Cardiomyopathy, myopathy, respiratory failure | Heart, skeletal muscle, nerves | Lapphund dog, mouse | AAV, Ad, LV |
III/Cori, Forbes | Debrancher | hepatomegaly, hypoglycemia, hyperlipidemia, and growth retardation | Liver, heart, skeletal muscles | Curly coated retriever dog, mouse | None |
IV/Anderson | Branching | Hepatosplenomegaly, failure to thrive | Liver, heart, nerves | Norwegian forest cat, mouse | None |
V/McArdle | Muscle phosphorylase | Exercise intolerance, muscle cramps | Skeletal muscle | Charlois cattle, sheep, mouse | AAV, Ad |
VII/Tarui | Phosphofructokinase | Exercise intolerance, muscle cramps, hemolytic anemia | Skeletal muscle, erythrocytes | English Springer spaniel dog, mouse | None |