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...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in pediatrics Vol. 9; p. 536730
Main Authors Belcher, Ryan, Virgin, Frank, Duis, Jessica, Wootten, Christopher
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 22.03.2021
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary: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.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
Edited by: Nagwa Elsayed Afify Gaboon, Ain Shams University, Egypt
Reviewed by: Avinash Vijay Dharmadhikari, Columbia University, United States; Bruna De Felice, University of Campania Luigi Vanvitelli, Italy
This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Pediatrics
ISSN:2296-2360
2296-2360
DOI:10.3389/fped.2021.536730