Article
Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière's Disease.
Archives of Iranian medicine - 1 May 2020
Mehrjoo Zohreh, Kahrizi Kimia, Mohseni Marzieh, Akbari Mojdeh, Arzhangi Sanaz, Jalalvand Khadijeh, Najmabadi Hossein, Farhadi Mohammad, Mohseni Mohammad, Asghari Alimohamad, Mohebbi Saleh, Daneshi Ahmad
Abstract excerpt
BACKGROUND: Ménière's disease (MD) is a common inner ear disorder which is characterized by recurrent attacks of vertigo, fluctuating sensorineural hearing loss (SNHL), tinnitus, and a sense of fullness in the affected ear. MD is a complex disorder; although six genes have been linked to familial autosomal dominant form of the disease, in many cases, the exact genetic etiology remains elusive. METHODS: To...
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