Glycogen storage disease: Difference between revisions

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(Created page with "{| class="wikitable" !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 tes...")
 
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* Liver transplantation
* Liver transplantation
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|GSD IV
|GSD IV (Andersen disease)
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Latest revision as of 15:29, 16 November 2022

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
  • No specific treatment
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
  • No specific treatment
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
  • No specific treatment
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
  • No specific treatment
GSD XI lactate dehydrogenase A (LDHA) deficiency and lactate dehudogenase B (LDHB) deficiency
  • Fatigability
  • Myoglobinuria
  • Rhabdomyolysis
  • Muscle or RBC enzyme assay
  • DNA testing
  • No specific treatment
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
  • No specific treatment
GSD XIII beta-enolase deficiency in muscle
  • Exercise intolerance
  • Increased CPK
  • Rhabdomyolysis
  • Muscle biopsy
  • Enzyme assay
  • DNA testing
  • No specific treatment
GSD XIV phosphoglucomutase 1 deficiency in muscle
  • Exercise intolerance
  • Myoglobinuria
  • Increased CPK
  • Rhabdomyolysis
  • Myoglobinuria
  • Muscle biopsy
  • Enzyme assay
  • DNA testing
  • No specific treatment
GSD XV glycogenin 1 deficiency in muscle
  • Muscle weakness
  • Arrhythmias
  • Muscle biopsy (glycogen depletion)
  • DNA testing
  • No specific treatment