Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy

Neurology. 2004 Dec 28;63(12):2376-9. doi: 10.1212/01.wnl.0000149498.79541.49.

Abstract

Background: Of the more than 40 genetically defined dominantly inherited hearing loss syndromes, only a few are associated with bilateral vestibulopathy. No genetic mutations have been identified in families with bilateral vestibulopathy and normal hearing.

Objective: To perform a genome-wide scan for linkage in four families with dominantly inherited bilateral vestibulopathy.

Methods: Patients in four families reported brief episodes of vertigo followed by imbalance and oscillopsia. Bilateral vestibulopathy was documented with quantitative rotational testing. Most patients with bilateral vestibulopathy also had migraine. A 10 cM genome-wide screen was conducted using 423 microsatellite markers to identify linkage with vestibulopathy.

Results: The authors identified a 24 cM region on chromosome 6q suggestive of linkage to vestibulopathy in these four families (maximum lod score of 2.9 at marker D6S1556). A small fifth family with a different phenotype was not linked to this region on chromosome 6q.

Conclusions: This is the first report of linkage in families with dominantly inherited vestibulopathy and normal hearing. Genetic heterogeneity is likely with inherited vestibulopathy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromosomes, Human, Pair 6 / genetics*
  • Female
  • Genes, Dominant
  • Genetic Heterogeneity
  • Haplotypes
  • Humans
  • Lod Score
  • Male
  • Microsatellite Repeats
  • Pedigree
  • Phenotype
  • Vertigo / genetics
  • Vestibular Diseases / genetics*