The cerebellopontine angle may show the bilateral absence of cochleovestibular
nerve with otherwise normal cerebral and cerebellar structures Branchiooculofacial Autosomal dominant condition TFAP2A characterized by branchial skin defects, ocular anomalies such as cataract, facial anomalies, malformed pinnae, and HL.
physiology is affected by the autonomic nervous system.
A new classification for cochleovestibular
The ear with normal anatomy is given preference over the ear with abnormal radiologically detected inner ear or cochleovestibular
All children with meningitis (n = 11) and 46% with cochleovestibular
radiological abnormalities (n=31) presented a dysfunction of the CSH, while 45% and 46%, respectively, showed saccular dysfunction.
Johnson, "Methotrexate management of immune-mediated cochleovestibular
disorders," Otolaryngology and Head and Neck Surgery, vol.
Cogan's syndrome (CS) is a rare chronic inflammatory disease, characterized by nonsyphilitic ocular keratitis and Meniere-like cochleovestibular
dysfunction, with relapsing attacks of vertigo, sudden onset of tinnitus, vomiting, and progressive, mostly bilateral sensorineural hearing loss .
Saatci, "A new classification for cochleovestibular
malformations," The Laryngoscope, vol.
Typically, RHS is characterized by zoster oticus, facial nerve palsy, and cochleovestibular
Radiological assessment by HRCT temporal bone and MRI head with 3D reconstruction of cochleovestibular
complex to see the status of
Clinically, it has been prescribed to treat dementia, vaso-occlusion, and cochleovestibular
disorders (Diamond et al.