Mcardle | search
Click here to view Mcardle news from 60+ newspapers.
Bookmark or Share- McArdle Disease - StatPearls - NCBI BookshelfMcArdle disease, also known as glycogen storage disorder (GSD) type V, is an inborn metabolic disorder characterized by a deficiency or complete absence of an enzyme called muscle glycogen phosphorylase (or myophosphorylase).
- McArdle disease | Description, Symptoms, & Treatment | BritannicaMcArdle disease, rare hereditary deficiency of the enzyme glycogen phosphorylase in muscle cells. In the absence of this enzyme, muscles cannot break down glycogen to meet the energy requirements of exercise. Learn more about the cause, symptoms, and treatment of McArdle disease.
- McArdle disease - Muscular Dystrophy UKMcArdle disease is a metabolic muscle disorder first described in 1951 by Dr Brian McArdle. The disorder is also called Glycogen Storage Disease Type V (GSD V). People born with McArdle disease are unable to produce an enzyme called muscle phosphorylase.
- McArdle Disease (GSD5): What It Is, Symptoms & Treatment - Cleveland ClinicMcArdle disease happens when you have a deficiency or complete lack of an enzyme called muscle glycogen phosphorylase (myophosphorylase). This issue causes symptoms like painful muscle cramps and weakness, especially during physical activity.
- Glycogen storage disease type V - MedlinePlusGlycogen storage disease type V (also known as GSDV or McArdle disease) is an inherited disorder caused by an inability to break down a complex sugar called glycogen in muscle cells. Explore symptoms, inheritance, genetics of this condition.
More
