Glycogen storage diseases (GSD): classification

Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .

Glycogen storage diseases (GSD): classification. This is caused by glycogen synthase deficiency. Fully referenced neurology checklist.

GSD type 0

  • This is caused by glycogen synthase deficiency
  • It is not a true GSD because there is reduced liver glycogen content

GSD type I

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GSD type II

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GSD type III

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GSD type IV

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GSD type V

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GSD type VI

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GSD type VII

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GSD type VIII

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GSD type IX

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GSD type X

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GSD type XI

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References

  1. van Adel BA, Tarnopolsky MA. Metabolic myopathies: update 2009. J Clin Neuromuscul Dis 2009; 10:97-121.
  2. DiMauro S, Spiegel R. Progress and problems in muscle glycogenoses. Acta Myol 2011; 30:96-102.
  3. Ozen H. Glycogen storage diseases: new perspectives. World J Gastroenterol 2007; 13:2541-2553.

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