Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy

Neuromuscul Disord. 2001 Nov;11(8):699-702. doi: 10.1016/s0960-8966(01)00227-9.

Abstract

The question whether oculopharyngodistal myopathy (MIM 164310) is a distinct disease entity or a variant of oculopharyngeal muscular dystrophy (MIM 164300) persists. To answer this question, we examined five patients with the clinical characteristics of oculopharyngodistal myopathy for GCG expansion in poly(A)-binding protein nuclear 1 gene (previously called poly(A)-binding protein 2), the causative gene defect for oculopharyngeal muscular dystrophy. Only one of our five patients had the significant GCG expansion. Thus, oculopharyngodistal myopathy is a genetically heterogeneous disorder, which includes patients with oculopharyngeal muscular dystrophy but, for the most part, is different genetically from oculopharyngeal muscular dystrophy.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Aged, 80 and over
  • Diagnosis, Differential
  • Female
  • Genetic Heterogeneity*
  • Humans
  • Male
  • Middle Aged
  • Muscular Diseases / diagnosis*
  • Muscular Diseases / genetics*
  • Muscular Dystrophies / diagnosis*
  • Muscular Dystrophies / genetics
  • Poly(A)-Binding Proteins
  • RNA-Binding Proteins / genetics
  • Trinucleotide Repeat Expansion / genetics

Substances

  • Poly(A)-Binding Proteins
  • RNA-Binding Proteins