Glycogen storage diseases (GSD): classification

Evidence-based neurology checklist on glycogen storage diseases (gsd): classification: 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 GSD type II GSD type III GSD type IV GSD type V GSD type VI GSD type VII…

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

GSD type II

GSD type III

GSD type IV

GSD type V

GSD type VI

GSD type VII

GSD type VIII

GSD type IX

GSD type X

GSD type XI

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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