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Article

Permanent muscle weakness in McArdle disease.

Muscle & nerve - 1 Sept 2009

Nadaj-Pakleza Aleksandra A, Vincitorio Carlo M, Laforêt Pascal, Eymard Bruno, Dion Elisabeth, Teijeira Susana, Vietez Irene, Jeanpierre Marc, Navarro Carmen, Stojkovic Tanya

Abstract excerpt

McArdle disease is an autosomal recessive muscle glycogenosis. In the typical clinical presentation, only exercise-related symptoms are noted. Nevertheless, permanent weakness may occur, usually late in life. In this study we report on the clinical and genetic features of fixed muscle weakness in...

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Source

Identifiers

PMID: 19670320
DOI: 10.1002/mus.21351

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19670320-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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