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Duplicated internal auditory canal with inner ear malformation: Case report and literature review.
- Source :
-
Auris, nasus, larynx [Auris Nasus Larynx] 2018 Apr; Vol. 45 (2), pp. 351-357. Date of Electronic Publication: 2017 Apr 23. - Publication Year :
- 2018
-
Abstract
- Internal auditory canal anomalies are rare. Narrow internal auditory canal is believed to occur as a result of aplasia or hypoplasia of the vestibulocochlear nerve. Narrow duplication of the internal auditory canal is considered to be very rare. Narrow duplication of the internal auditory canal with inner ear malformation has been reported in only 3 cases. We present 2 cases of narrow duplication of the internal auditory canal with inner ear malformation. The first case had inner ear malformation on only one side and the second case had inner ear malformation on both sides. The embryogenesis may be different between internal auditory canal and inner ear.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Subjects :
- Audiometry, Pure-Tone
Child
Cochlea abnormalities
Cochlea diagnostic imaging
Ear, Inner diagnostic imaging
Evoked Potentials, Auditory, Brain Stem
Female
Hearing Loss, Bilateral congenital
Hearing Loss, Bilateral physiopathology
Hearing Loss, Unilateral congenital
Hearing Loss, Unilateral physiopathology
Humans
Imaging, Three-Dimensional
Infant
Magnetic Resonance Imaging
Male
Otoacoustic Emissions, Spontaneous
Semicircular Canals abnormalities
Semicircular Canals diagnostic imaging
Temporal Bone abnormalities
Temporal Bone diagnostic imaging
Tomography, X-Ray Computed
Vestibule, Labyrinth abnormalities
Vestibule, Labyrinth diagnostic imaging
Ear, Inner abnormalities
Hearing Loss, Bilateral diagnostic imaging
Hearing Loss, Unilateral diagnostic imaging
Subjects
Details
- Language :
- English
- ISSN :
- 1879-1476
- Volume :
- 45
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Auris, nasus, larynx
- Publication Type :
- Academic Journal
- Accession number :
- 28446373
- Full Text :
- https://doi.org/10.1016/j.anl.2017.03.019