McArdle's disease: The unsolved mystery of the reappearing enzyme

Andrea Martinuzzi, Giuliana Schievano, Annachiara Nascimbeni, Marina Fanin

Research output: Contribution to journalArticle

Abstract

We assessed the frequency of muscle fibers showing histochemical phosphorylase activity in 27 muscle biopsies from 25 unrelated patients with McArdle's disease and studied by immunohistochemistry and in situ hybridization whether the muscle-specific isoform was expressed. Positive phosphorylase fibers were observed in 19% of our series of biopsies. We show that the enzyme isoform expressed in regenerating fibers differs according to the genotype of patients: the muscle-specific isoform is transcribed and translated in patients with none of the described mutations in at least one allele of the myophosphorylase gene, whereas it is neither transcribed nor translated in patients with identified mutations in both alleles.

Original languageEnglish
Pages (from-to)1893-1897
Number of pages5
JournalAmerican Journal of Pathology
Volume154
Issue number6
Publication statusPublished - 1999

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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    Martinuzzi, A., Schievano, G., Nascimbeni, A., & Fanin, M. (1999). McArdle's disease: The unsolved mystery of the reappearing enzyme. American Journal of Pathology, 154(6), 1893-1897.