Meniere disease (MD) is a rare set of conditions associated with the accumulation of
endolymph in the cochlear duct and the vestibular labyrinth with a decrease of endocochlear …

Background: Vestibular disorders (VDs) are a clinically divergent group of conditions that
stem from pathology at the level of the inner ear, vestibulocochlear nerve, or central …

Objectives: Meniere's disease (MD) is a rare inner ear disorder characterized by
sensorineural hearing loss, episodic vertigo, and tinnitus. Familial MD has been reported in …

The MYO7A gene encodes a motor protein with a key role in the organization of stereocilia
in auditory and vestibular hair cells. Rare variants in the MYO7A (myosin VIIA) gene may …

Objective: In order to identify genetic variants associated with vestibular neuritis, a common
cause of peripheral vertigo with a potential causative link to the reactivation of herpes …

Hearing loss (HL) is the most common sensory deficit in humans and is frequently
accompanied by peripheral vestibular loss (PVL). While often overlooked, PVL is an …

Growing evidence supports the contribution of allelic variation to vestibular disorders.
Heritability attributed to rare allelic variants is found in familial vestibular syndromes such as …

Objectives: The cause of Meniere's disease (MD) is unclear but likely involves genetic and
environmental factors. The aim of this study was to investigate the genetic basis underlying …

Background: The vestibular phenotypes of patients with genetic hearing loss are poorly
understood. Methods: we performed genetic testing including exome sequencing and …

Objective In this study, clinical data from vestibular migraine (VM) patients and healthy
control populations were collected to analyze the clinical data of VM patients, especially the …