Objectives This article reviews the current role of genetics in pediatric hearing loss (HL).
Methods A review of the current literature regarding the genetic basis of HL in children was …

Hearing loss (HL), as a broad diagnostic term, affects upwards of 360 million people
worldwide. 1 However, the etiologic diversity of HL proves to be a challenge to efficient …

Hearing loss (HL) is a common and complex condition that can occur at any age, be
inherited or acquired, and is associated with a wide number of etiologies. HL is the most …

Hearing plays an important role in human development and childhood speech learning for
the proper functioning and development of people in society. Hearing loss (HL) is one of the …

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Hearing loss (HL) is an extremely common neurosensory deficit with a heterogeneous
etiology including environmental and genetic causes. The incidence of profound …

As knowledge regarding the genetic underpinnings of hearing loss has rapidly evolved, the
role of the clinician in managing the patient has expanded beyond that of defining the …

Hearing loss (HL) is the most common sensory impairment and is caused by a broad range
of inherited to environmental causes. Inherited HL consists 50–60% of all HL cases. The …

Genetic factors contribute significantly to congenital hearing loss, with non-syndromic cases
being more prevalent and genetically heterogeneous. Currently, 150 genes have been …

Hereditary hearing loss is clinically and genetically heterogeneous. There are presently over
120 genes that have been associated with non-syndromic hearing loss and many more that …