Molecular genetics of McArdle's disease.

A L Andreu, J Arenas, G Nogales-Gadea

Journal: Current neurology and neuroscience reports 2007;7(1):84-92

PMID: 17217859

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Abstract

This review highlights recent advances in our understanding of McArdle's disease, including the mechanisms involved in the regulation of the clinical phenotype. The latest molecular genetic studies have demonstrated the genetic heterogeneity of the disorder, with more than 65 mutations identified to date. There is not a specific treatment for McArdle's disease, but some nutritional treatments in combination with aerobic conditioning could improve the quality of life in most patients.

Address: Dept Patologia Mitocondrial i Neuromuscular, Centre d'Investigacions en Bioguimica y Bioloqía Molecular, Institut de Recera Vall d'Hebron, Barcelona, Spain.

DOI: 10.1007/s11910-007-0026-2

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MeSH Terms: Glycogen Phosphorylase, Muscle Form, Glycogen Storage Disease Type V, Humans, Molecular Biology, Mutation