Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

The genetics of vertigo.

Kevin A Kerber1

  • 1Departments of Neurology and Otolaryngology, University of Michigan Health System, Ann Arbor, Michigan 48109, USA. kakerber@umich.edu

Seminars in Neurology
|October 19, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Diagnosis and Treatment of Benign Paroxysmal Positional Vertigo.

JAMA·2026
Same author

Validity of Nonspecific Stroke Location ICD-10 Subcodes: A Descriptive Study.

Cerebrovascular diseases extra·2025
Same author

Cumulative Incidence of Stroke Disability and Mortality Following Emergency Department Discharge for Dizziness: A Cohort Study.

Annals of emergency medicine·2025
Same author

Dizziness and its effect on health-related quality of life (DRQOL).

Journal of vestibular research : equilibrium & orientation·2025
Same author

DIZZiness treatment through implementation and clinical strategy Tactics-2 (DIZZTINCT-2) project-a clinical trial protocol.

Trials·2025
Same author

Diagnostic Testing for Patients With Peripheral Neuropathy.

JAMA neurology·2025

Familial vertigo, often caused by inner ear or central nervous system disorders, presents unique genetic features. Understanding these genetic vertigo syndromes is key to diagnosis and treatment.

Area of Science:

  • Neurology
  • Otolaryngology
  • Genetics

Background:

  • Vertigo is a frequent complaint across medical specialties.
  • While benign inner ear issues are common, central nervous system causes require exclusion.
  • Familial vertigo syndromes are distinct due to their hereditary nature.

Purpose of the Study:

  • To provide an overview of familial vertigo.
  • To discuss clinical features, genetic analyses, and treatment strategies.
  • To highlight the importance of distinguishing familial causes.

Main Methods:

  • Review of clinical presentations of familial vertigo.
  • Analysis of genetic findings, including susceptibility loci and mutations.
  • Examination of current treatment approaches.

Related Experiment Videos

Main Results:

  • Familial vertigo is associated with isolated vertigo, deafness syndromes, and neurological disorders.
  • Genetic heterogeneity is a common characteristic of these syndromes.
  • Research has improved understanding of vertigo pathophysiology.

Conclusions:

  • Familial vertigo syndromes have identifiable genetic components.
  • Further research is needed to fully understand vertigo pathophysiology.
  • Clinical and genetic evaluation is crucial for managing vertigo.