Meniere disease (MD) is a rare disorder of the inner ear defined by sensorineural hearing
loss (SNHL) associated with episodes of vertigo and tinnitus. The phenotype is variable, and …

Ménière's disease (MD) is a rare syndromic disorder of the inner ear defined by
sensorineural hearing loss (SNHL) associated with episodes of vertigo and tinnitus. The …

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 …

Dear Editor Although there have been considerable advances in recent years, the
contribution of genetic factors to Meniere's disease (MD) is not yet fully understood. MD …

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 …

Meniere disease is a complex inner ear disorder with significant familial aggregation. A
differential prevalence of familial MD (FMD) has been reported, being 9–10% in Europeans …

Background In recent years, there has been an increasing number of publications on
Meniere's disease. However, there are no bibliometric research on Meniere's disease. The …

Familial Meniere Disease (FMD) is a rare polygenic disorder of the inner ear. Mutations in
the connexin gene family, which encodes gap junction proteins, can also cause hearing …

The 22q11. 2 deletion syndrome (22q11. 2DS), caused by a microdeletion on the long arm
of chromosome 22, is characterized by congenital heart disease, hypoparathyroidism …

Menière's disease (MD) is an episodic vertigo syndrome typically combining vestibular and
cochlear symptoms and signs. It is the second most frequent cause of peripheral and known …