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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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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. |
format | Online Article Text |
id | pubmed-7036719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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