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Asymmetrically severe internal auditory canal hypoplasia: A case report [PDF]

open access: yesRadiology Case Reports, 2020
We present a case of an otherwise healthy 20-month-old with congenital sensorineural hearing loss. CT and MR imaging demonstrated bilateral asymmetrically severe hypoplasia of the internal auditory canals and vestibulocochlear nerves.
Jeremy W. Martin   +6 more
doaj   +3 more sources

The vestibulocochlear nerve (VIII)

open access: yesDiagnostic and Interventional Imaging, 2013
The vestibulocochlear nerve (8th cranial nerve) is a sensory nerve. It is made up of two nerves, the cochlear, which transmits sound and the vestibular which controls balance. It is an intracranial nerve which runs from the sensory receptors in the internal ear to the brain stem nuclei and finally to the auditory areas: the post-central gyrus and ...
Benoudiba, F.   +2 more
openaire   +4 more sources

HISTOLOGICAL INVESTIGATION OF TRIGEMINAL V, ABDUCENT VI, FACIAL VII AND VESTIBULOCOCHLEAR VIII NERVE NUCLEI IN ONE HUMPED CAMEL ( Camelus Dromedarius ) [PDF]

open access: diamondBasrah Journal of Veterinary Research, 2008
The present work making histological investigation of certain part of medulla oblongata on seven one humped camel ( Camelus dromedarius ) in different ages and sexes, the Trigeminal V, Abducent VI, Facial VII, and Vestibulocochlear VIII nerve nuclei in ...
T.A.Abass
doaj   +2 more sources

Management of neurovascular compromise of the vestibulocochlear nerve: A systematic review and illustrative case series

open access: goldWorld Neurosurgery: X
Objective: To review the outcomes of surgery for asymmetric sensorineural hearing loss (ASHL) from neurovascular compromise of the vestibulocochlear nerve.
Vera Ong   +8 more
doaj   +2 more sources

Cranial Nerve Involvement With Diplopia as Presenting Feature of CMT1H Caused by Recurring FBLN5 Variant. [PDF]

open access: yesJ Peripher Nerv Syst
ABSTRACT Background and Aims CMT1H is a rare, autosomal dominant, demyelinating subtype of CMT caused by variants in FBLN5. Symptomatic cranial nerve involvement has never been reported in patients with CMT1H. Case Report We report a 45‐year‐old woman with a history of long‐standing diplopia.
Koutsis G   +11 more
europepmc   +2 more sources

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