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 …

Familial Meniere Disease (FMD) is a rare inner ear disorder characterized by episodic
vertigo associated with sensorineural hearing loss, tinnitus and/or aural fullness. We …

Meniere Disease (MD) is an idiopathic inner ear disease with complex etiology and
pathogenesis, which is still unclear. With the development in gene analysis technology, the …

While it has attracted emerging attention in recent years, the study of Meniere's disease
genetics is still at its early stage. More geographically and ethnically based human genome …

Objectives/Hypothesis This study was undertaken to investigate the prevalence, inheritance
patterns, and clinical characteristics of familial Meniere's disease (MD) in a South Korean …

Meniere's disease (MD) is a complex disorder of the inner ear that causes vertigo attacks,
fluctuating sensorineural hearing loss (SNHL), tinnitus and aural fullness. MD has been …

Meniere's disease (MD) is a clinical spectrum of rare disorders characterized by vertigo
attacks, associated with sensorineural hearing loss (SNHL) and tinnitus involving low to …

Objective: Ménière's disease (MD) is a chronic illness characterized by sensorineural
hearing loss, recurring vertigo attacks, and tinnitus. It is possibly of multifactorial origin …

Our understanding of the genetic basis of Ménière's disease (MD) is still limited. Although
the familial clustering and the geographical and racial differences in incidence strongly …

Objective: Multiple candidate genes have been presented for Ménière's disease (MD), but to
date no positive replications have been reported. We review here all the previously …