A diagnostic protocol for adult-onset glycogen storage disease type II

Neurology. 1999 Mar 10;52(4):851-3. doi: 10.1212/wnl.52.4.851.

Abstract

To analyze the diagnostic value of various laboratory tests for the confirmation of adult-onset glycogen storage disease type II (GSD II), we performed a clinical, biochemical, and genetic study of 18 patients with this disease. Measurement of acid alpha-glucosidase (GAA) activity in muscle and histopathologic analysis of muscle tissue appeared to have no additional value when GAA activity in leukocytes was clearly deficient. Our study showed that creatine kinase elevation is a sensitive marker of GSD II. A diagnostic protocol is formulated.

MeSH terms

  • Age of Onset
  • Electromyography
  • Glucosidases / metabolism*
  • Glycogen Storage Disease Type II / diagnosis*
  • Glycogen Storage Disease Type II / genetics
  • Humans
  • Leukocytes / enzymology
  • Muscles / enzymology
  • Muscles / physiopathology

Substances

  • Glucosidases