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Glycogen Storage Diseases (GSD): An Overview

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    AMA Citation
    Glycogen Storage Diseases (GSD): An Overview. In: Bissonnette B, Luginbuehl I, Marciniak B, Dalens BJ. Bissonnette B, Luginbuehl I, Marciniak B, Dalens B.J. Eds. Bruno Bissonnette, et al.eds. Syndromes: Rapid Recognition and Perioperative Implications New York, NY: McGraw-Hill; 2006. http://accessanesthesiology.mhmedical.com/content.aspx?bookid=852&sectionid=49517613. Accessed April 19, 2019.
    MLA Citation
    . "Glycogen Storage Diseases (GSD): An Overview." Syndromes: Rapid Recognition and Perioperative Implications Bissonnette B, Luginbuehl I, Marciniak B, Dalens BJ. Bissonnette B, Luginbuehl I, Marciniak B, Dalens B.J. Eds. Bruno Bissonnette, et al. New York, NY: McGraw-Hill, 2006, http://accessanesthesiology.mhmedical.com/content.aspx?bookid=852&sectionid=49517613.

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Table G-3.

Table G-3 Glycogen Storage Disease (GSD): An Overview
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Table G-3 Glycogen Storage Disease (GSD): An Overview
GSD no.Deficient Enzymatic ActivityEponym
IGlucose-6-phosphatase IVon Gierke disease
IIAlpha 1,4-glucosidase (acid maltase)Pompe disease
IIIDebrancher (amylo-1,6 glucosidase)Cori disease
IVBrancherAndersen disease
VMuscle phosphorylaseMcArdle disease
VILiver phosphorylaseHers disease
VIIPhosphofructokinaseTarui disease
VIIIPhosphorylase kinase of liver

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