Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13

Ann Neurol. 1996 Nov;40(5):801-4. doi: 10.1002/ana.410400519.

Abstract

Oculopharyngeal muscular dystrophy is a late-onset, autosomally dominant disorder characterized by progressive ptosis, dysphagia, and extremity weakness. Linkage of oculopharyngeal muscular dystrophy to 14q11.2-q13 has been reported in a series of French Canadian families. Haplotype analysis in these data shows a single segregating disease chromosome, suggesting a founder effect in this population. We ascertained and sampled for linkage studies 5 multigenerational American families with oculopharyngeal muscular dystrophy. Four of the 5 families have known French Canadian ancestry while the fifth is of English/Scottish origin. A peak multipoint lod score of 6.30 was obtained for the marker MYH7.1 in the families, confirming linkage to 14q11.2-q13. The English/Scottish family exhibited a different chromosomal haplotype for the oculopharyngeal muscular dystrophy alleles than did the families of French Canadian origin. These data suggest that this family may represent a second, possibly independent mutation in this disorder.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Age of Onset
  • Alleles
  • Canada
  • Chromosome Mapping
  • Chromosomes, Human, Pair 14*
  • Confidence Intervals
  • England / ethnology
  • France / ethnology
  • Genetic Linkage
  • Genetic Markers
  • Haplotypes
  • Humans
  • Lod Score
  • Muscular Dystrophies / classification
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophies / physiopathology
  • Oculomotor Muscles
  • Pharyngeal Muscles
  • Scotland / ethnology

Substances

  • Genetic Markers