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Article
June 1983

Late-Onset McArdle's Disease With Unusual Electromyographic Findings

Author Affiliations

From the Department of Neurology, University of Virginia School of Medicine and the University of Virginia Jerry Lewis Neuromuscular Center, Charlottesville. Dr Pourmand is now with Indiana University School of Medicine, Indianapolis. Dr Sanders is now with Duke University Medical Center, Durham, NC.

Arch Neurol. 1983;40(6):374-377. doi:10.1001/archneur.1983.04050060074014
Abstract

• Symptoms of McArdle's disease (muscle phosphorylase deficiency) commonly begin in childhood or adolescence. Late onset of the disease is rare. We describe a 76-year-old man whose symptoms began at age 74 years with sudden onset of proximal muscle weakness and fatigability. Electromyography disclosed substantial spontaneous activity and myopathic features as seen in inflammatory muscle disease. The diagnosis of McArdle's disease was made by histochemical studies of muscle, an abnormal ischemic lactate test, and absence of myophosphorylase activity.

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