Glycogen Storage Disease Type V
Glycogen storage disease type V (GSD-V) is a metabolic disorder, more specifically a glycogen storage disease, caused by a deficiency of myophosphorylase. Its incidence is reported as 1 in 100,000, approximately the same as glycogen storage disease type I.
GSD type V is also known as McArdle disease or muscle phosphorylase (myophosphorylase) deficiency. The disease was first reported in 1951 by Dr. Brian McArdle of Guy's Hospital, London.
Read more about Glycogen Storage Disease Type V: History, Symptoms and Presentation, Laboratory Tests, Treatment/Therapy, Genetic Basis, The Reaction
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