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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Published in | Frontiers in pediatrics Vol. 9; p. 536730 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
22.03.2021
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Subjects | |
Online Access | Get full text |
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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. |
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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 |