Semin Neurol 2006; 26(5): 484-491
DOI: 10.1055/s-2006-951620
Copyright © 2006 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA.

The Genetics of Vertigo

Kevin A. Kerber1
  • 1Departments of Neurology and Otolaryngology, University of Michigan Health System, Ann Arbor, Michigan
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Publikationsverlauf

Publikationsdatum:
17. Oktober 2006 (online)

ABSTRACT

Vertigo is a common principal complaint among patients seen by primary care physicians, neurologists, and otolaryngologists. The most common causes of recurrent episodes of vertigo are benign inner ear disorders, but central nervous system disorders must be excluded. Several common vertigo syndromes are now known to be familial, a feature distinguishing them from other common causes of vertigo. Familial vertigo has been recognized in patients with isolated recurrent attacks of vertigo, genetic deafness syndromes, and in patients with neurological disorders. Although susceptibility loci and mutations have been identified, genetic heterogeneity is common in all familial vertigo syndromes. Research in these disorders has advanced the understanding of vertigo pathophysiology but much remains to be known. This article provides an overview of the clinical features, genetic analyses, and treatment strategies for these disorders.

REFERENCES

Kevin A Kerber, M.D. 

Department of Neurology, University of Michigan Medical School

1500 East Medical Center Drive, TC 1920/0316, Ann Arbor, MI 48109-0316

eMail: [email protected]