McArdle disease- Glycogen Storage Disease type V (GSD-V) - Clinical Biochemistry & Genetics

McArdle disease- Glycogen Storage Disease type V (GSD-V) - Clinical Biochemistry & Genetics.
Deficiency of the muscle glycogen phosphorylase enzyme. Normally, this enzyme breaks down the glycogen in the muscle into glucose-6-phosphate (for muscle use only). McArdle disease is associated with muscle weakness.
Glycogen Storage Disease (Type IV) - Learn about Glycogen Metabolism, Glycogen synthesis (Glycogenesis) and Glycogen breakdown (Glycogenolysis) - Metabolism - Clinical Biochemistry for doctors, nurses, pharmacists, physician assistants, dietitians, and premed students.
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McArdle disease does not cause muscle weakness, it causes muscle exhaustion due to lack of fuel. Once fuel is provided by circulation, known as second wind, we can use resistance training to build strong muscles. Rhabdomyolysis is only experienced by a small proportion of McArdle disease patients. Lactate is used as fuel in McArdle disease, so does not show up in serum. McArdle disease is characterized as activity of daily living intolerance.

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