Class
|
Defect
|
Clinical Clues
|
Diagnosis
|
Therapy
|
GSD 0a
|
Glycogen synthase 2 deficiency in liver
|
- Ketotic hypoglycemia
- No hepatomegaly
|
- Liver biopsy and enzyme testing
- DNA testing
|
- Uncooked cornstarch
- Commercial glucose polymers (eg, Glycosade)
- Liver transplantation
|
GSD 0b
|
muscle glycogen synthase deficiency
|
- Cardiomyopathy
- Exercise intolerance
- Weakness
|
- Muscle biopsy (glycogen depletion)
- Enzyme assay
- DNA testing
|
|
GSD Ia (von Gierke disease)
|
glucose-6-phosphatase deficiency
|
- Ketotic hypoglycemia
- Hepatomegaly
|
- DNA testing
- Liver biopsy
- Enzyme assay
|
- Uncooked cornstarch
- Allopurinol
- Granulocyte colony-stimulating factor (G-CSF)
- Commercial glucose polymers (eg, Glycosade)
- Liver transplantation
|
GSD Ib
|
q transport defect
|
GSD II (Pompe disease)
|
lysosomal acid maltase deficiency
|
- Hypotonia
- Muscle weakness
- Hypertrophic cardiomyopathy
- Rhabdomyolysis
|
- Fibroblast, leukocyte, muscle, or liver enzyme assay
- DNA testing
|
- Enzyme replacement therapy
- Commercial glucose polymers (eg, Glycosade)
- Liver transplantation
|
GSD IIb (Danon disease)
|
lysosome-associated membrane protein 2 (LAMP2) deficiency
|
- Hypotonia
- Hypertrophic cardiomyopathy
- Rhabdomyolysis
|
- Muscle biopsy
- DNA testing
|
|
GSD III
|
glycogen debrancher deficiency
|
- Ketotic hypoglycemia
- Hepatomegaly
|
- Fibroblast or liver enzyme assay
- DNA testing
|
- Uncooked cornstarch
- Commercial glucose polymers (eg, Glycosade)
- Liver transplantation
|
GSD IV (Andersen disease)
|
glycogen branching enzyme deficiency
|
- Hepatomegaly
- Cirrhosis
- Rare neuromuscular presentations, such as fetal akinesia sequence, myopathy, axonal neuropathy, adult polyglucosan body disease
|
- Fibroblast, muscle, or liver biopsy
- DNA testing
|
- Commercial glucose polymers (eg, Glycosade)
- Liver transplantation
|
GSD V (McArdle disease)
|
muscle phosphorylase deficiency
|
- Fatigability
- Myoglobinuria
- Rhabdomyolysis
|
- Muscle biopsy
- Muscle enzyme assay
- DNA testing
|
- Sucrose prior to exercise
|
GSD VI (Hers disease)
|
liver phosphorylase deficiency
|
- Hepatomegaly
- Mild hypoglycemia
|
- Liver biopsy and enzyme assay
- DNA testing
|
- Commercial glucose polymers (eg, Glycosade)
- Liver transplantation
|
GSD VII (Tarui disease)
|
phosphofructokinase deficiency in muscle
|
- Fatigability
- Myoglobinuria
- Rhabdomyolysis
|
- Muscle enzyme assay
- DNA testing
|
|
Phosphoglycerate kinase deficiency
|
phosphoglycerate kinase deficiency
|
- Hemolysis
- Fatigability
- Myoglobinuria
- CNS dysfunction
- Rhabdomyolysis
|
- Muscle/RBC enzyme assay
- DNA testing
|
- Bone marrow transplantation
|
GSD IX
|
phosphorylase kinase deficiency
|
- Hepatomegaly
- Mild hypoglycemia
- Fatigability
- Exercise intolerance
|
- Liver/muscle biopsy
- Enzyme assay
- DNA testing
|
- Commercial glucose polymers (eg, Glycosade)
- Liver transplantation
|
GSD IXa1 (GSD VII)
|
alpha-2 subunit defect in liver
|
GSD IXb
|
beta subunit defect in liver
|
GSDIXc
|
gamma subunit defect in liver and muscle
|
GSD IXd
|
alpha subunit defect in muscle
|
GSD X
|
phosphoglycerate mutase deficiency
|
- Fatigability
- Myoglobinuria
- Exercise intolerance
- Rhabdomyolysis
|
- Muscle biopsy and enzyme assay
- DNA testing
|
|
GSD XI
|
lactate dehydrogenase A (LDHA) deficiency and lactate dehudogenase B (LDHB) deficiency
|
- Fatigability
- Myoglobinuria
- Rhabdomyolysis
|
- Muscle or RBC enzyme assay
- DNA testing
|
|
Fanconi-Bickel syndrome
|
GLUT2 deficiency
|
- Growth retardation
- Renal Fanconi syndrome
- Galactosemia
|
- Clinical features
- DNA testing
|
- Frequent, small meals
- Uncooked cornstarch or nocturnal enteral nutrition
- Electrolytes, carnitine, and vitamin D as needed
- Restriction of galactose
|
GSD XII
|
aldolase A deficiency
|
- Hemolysis
- Jaundice
- Myoglobinuria
- Muscle weakness
- Fatigability
- Rhabdomyolysis
|
- Muscle or RBC enzyme assay
- DNA testing
|
|
GSD XIII
|
beta-enolase deficiency in muscle
|
- Exercise intolerance
- Increased CPK
- Rhabdomyolysis
|
- Muscle biopsy
- Enzyme assay
- DNA testing
|
|
GSD XIV
|
phosphoglucomutase 1 deficiency in muscle
|
- Exercise intolerance
- Myoglobinuria
- Increased CPK
- Rhabdomyolysis
- Myoglobinuria
|
- Muscle biopsy
- Enzyme assay
- DNA testing
|
|
GSD XV
|
glycogenin 1 deficiency in muscle
|
- Muscle weakness
- Arrhythmias
|
- Muscle biopsy (glycogen depletion)
- DNA testing
|
|