Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss

Hearing loss is one of the most common concerns for presentation for a geneticist. Presentation prior to the age of one (congenital hearing loss), profound sensorineural hearing loss (SNHL), and bilateral hearing loss are sensitive and should raise concern for genetic causes of hearing loss and prom...

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Autores principales: Belcher, Ryan, Virgin, Frank, Duis, Jessica, Wootten, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020033/
https://www.ncbi.nlm.nih.gov/pubmed/33829002
http://dx.doi.org/10.3389/fped.2021.536730
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author Belcher, Ryan
Virgin, Frank
Duis, Jessica
Wootten, Christopher
author_facet Belcher, Ryan
Virgin, Frank
Duis, Jessica
Wootten, Christopher
author_sort Belcher, Ryan
collection PubMed
description Hearing loss is one of the most common concerns for presentation for a geneticist. Presentation prior to the age of one (congenital hearing loss), profound sensorineural hearing loss (SNHL), and bilateral hearing loss are sensitive and should raise concern for genetic causes of hearing loss and prompt referral for genetic testing. Genetic testing particularly in this instance offers the opportunity for anticipatory guidance including possible course of the hearing loss over time and also connection and evaluation for additional congenital anomalies that may be associated with an underlying syndrome vs. isolated genetic hearing loss.
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spelling pubmed-80200332021-04-06 Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss Belcher, Ryan Virgin, Frank Duis, Jessica Wootten, Christopher Front Pediatr Pediatrics Hearing loss is one of the most common concerns for presentation for a geneticist. Presentation prior to the age of one (congenital hearing loss), profound sensorineural hearing loss (SNHL), and bilateral hearing loss are sensitive and should raise concern for genetic causes of hearing loss and prompt referral for genetic testing. Genetic testing particularly in this instance offers the opportunity for anticipatory guidance including possible course of the hearing loss over time and also connection and evaluation for additional congenital anomalies that may be associated with an underlying syndrome vs. isolated genetic hearing loss. Frontiers Media S.A. 2021-03-22 /pmc/articles/PMC8020033/ /pubmed/33829002 http://dx.doi.org/10.3389/fped.2021.536730 Text en Copyright © 2021 Belcher, Virgin, Duis and Wootten. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Belcher, Ryan
Virgin, Frank
Duis, Jessica
Wootten, Christopher
Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
title Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
title_full Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
title_fullStr Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
title_full_unstemmed Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
title_short Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
title_sort genetic and non-genetic workup for pediatric congenital hearing loss
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020033/
https://www.ncbi.nlm.nih.gov/pubmed/33829002
http://dx.doi.org/10.3389/fped.2021.536730
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