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Compelling evidence indicates that some newborns harboring genetic variants associated with hearing loss might not be identified by current physiologic newborn hearing screening (NBHS) rendering current NBHS protocols suboptimal. Incorporating… Click to show full abstract
Compelling evidence indicates that some newborns harboring genetic variants associated with hearing loss might not be identified by current physiologic newborn hearing screening (NBHS) rendering current NBHS protocols suboptimal. Incorporating genomic sequencing into NBHS would improve clinical diagnosis and decrease time to early intervention efforts.
Keywords:
genetics childhood;
genetics;
childhood hearing;
hearing loss
Journal Title: Otolaryngologic clinics of North America
Year Published: 2021
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Journal Title: Otolaryngologic clinics of North America
Year Published: 2021
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!