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Oculopharyngeal muscular dystrophy: A polyalanine myopathy

Current Neurology and Neuroscience Reports volume 9, pages 76–82 (2009)Cite this article

Abstract

It has been 10 years since the identification of the first PABPN1 gene (GCN)n/polyalanine mutations responsible for oculopharyngeal muscular dystrophy (OPMD). These mutations have been found in most cases of OPMD diagnosed in more than 35 countries. Sequence analyses have shown that such mutations have occurred numerous times in human history. Although PABPN1 was found early on to be a component of the classic filamentous intranuclear inclusions (INIs), mRNA and other proteins also have been found to coaggregate in the INIs. It is still unclear if the INIs play a pathologic or a protective role. The generation of numerous cell and animal models of OPMD has led to greater insight into its complex molecular pathophysiology and identified the first candidate therapeutic molecules. This paper reviews basic and clinical research on OPMD, with special emphasis on recent developments in the understanding of its pathophysiology.

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Authors and Affiliations

  1. Laboratory of Neurogenetics of Motion, Faculty of Medicine, University of Montreal, CHUM Research Center, M-4211-L3, 1560, Sherbrooke East, Montreal, QC, H2L 4M1, Canada

    Bernard Brais

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Correspondence to Bernard Brais.

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Brais, B. Oculopharyngeal muscular dystrophy: A polyalanine myopathy. Curr Neurol Neurosci Rep 9, 76–82 (2009). https://doi.org/10.1007/s11910-009-0012-y

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  • DOI: https://doi.org/10.1007/s11910-009-0012-y

Keywords

  • Muscular Dystrophy
  • Inclusion Body Myositis
  • Polyalanine
  • Levator Palpebrae
  • Centronuclear Myopathy