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Asymmetrically severe internal auditory canal hypoplasia: A case report

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. Additional developmental inner ear anomalies were present in this...

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Autores principales: Martin, Jeremy W., Wishka, Christian, Thompson, Matthew, Djalilian, Hamid R., Floriolli, David, Senturk, Cagin, Hasso, Anton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036719/
https://www.ncbi.nlm.nih.gov/pubmed/32123553
http://dx.doi.org/10.1016/j.radcr.2020.01.037
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author Martin, Jeremy W.
Wishka, Christian
Thompson, Matthew
Djalilian, Hamid R.
Floriolli, David
Senturk, Cagin
Hasso, Anton
author_facet Martin, Jeremy W.
Wishka, Christian
Thompson, Matthew
Djalilian, Hamid R.
Floriolli, David
Senturk, Cagin
Hasso, Anton
author_sort Martin, Jeremy W.
collection PubMed
description 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. Additional developmental inner ear anomalies were present in this patient, including unilateral semicircular canal hypoplasia and suspected bilateral cochlear hypoplasia. The patient retained normal facial nerve function bilaterally. We highlight the current research and understanding of congenital IAC abnormalities.
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spelling pubmed-70367192020-03-02 Asymmetrically severe internal auditory canal hypoplasia: A case report Martin, Jeremy W. Wishka, Christian Thompson, Matthew Djalilian, Hamid R. Floriolli, David Senturk, Cagin Hasso, Anton Radiol Case Rep Neuroradiology 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. Additional developmental inner ear anomalies were present in this patient, including unilateral semicircular canal hypoplasia and suspected bilateral cochlear hypoplasia. The patient retained normal facial nerve function bilaterally. We highlight the current research and understanding of congenital IAC abnormalities. Elsevier 2020-02-22 /pmc/articles/PMC7036719/ /pubmed/32123553 http://dx.doi.org/10.1016/j.radcr.2020.01.037 Text en © 2020 The Authors. Published by Elsevier Inc. on behalf of University of Washington. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Neuroradiology
Martin, Jeremy W.
Wishka, Christian
Thompson, Matthew
Djalilian, Hamid R.
Floriolli, David
Senturk, Cagin
Hasso, Anton
Asymmetrically severe internal auditory canal hypoplasia: A case report
title Asymmetrically severe internal auditory canal hypoplasia: A case report
title_full Asymmetrically severe internal auditory canal hypoplasia: A case report
title_fullStr Asymmetrically severe internal auditory canal hypoplasia: A case report
title_full_unstemmed Asymmetrically severe internal auditory canal hypoplasia: A case report
title_short Asymmetrically severe internal auditory canal hypoplasia: A case report
title_sort asymmetrically severe internal auditory canal hypoplasia: a case report
topic Neuroradiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036719/
https://www.ncbi.nlm.nih.gov/pubmed/32123553
http://dx.doi.org/10.1016/j.radcr.2020.01.037
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