Results 1 to 10 of about 71,647 (266)

Trajectory of hearing loss in children with unilateral hearing loss

open access: yesFrontiers in Pediatrics, 2023
IntroductionThe aim of this study was to quantify the amount of deterioration in hearing and to document the trajectory of hearing loss in early identified children with unilateral hearing loss (UHL).
Elizabeth M. Fitzpatrick   +12 more
doaj   +4 more sources

Evaluation of the Recovery of Idiopathic Sudden Sensorineural Hearing Loss Based on Estimated Hearing Disorders

open access: yesAudiology Research, 2022
Various prognostic factors for idiopathic sudden sensorineural hearing loss (SSNHL) have been reported. Hearing loss directly derived from idiopathic SSNHL is important for understanding underlying pathogenesis and outcomes. We assessed the usefulness of
Tadashi Nishimura   +5 more
doaj   +1 more source

Hearing loss in the pediatric age group

open access: yesSahel Medical Journal, 2020
Background: Hearing loss is one of the preventable diseases listed by the WHO, even though the prevalence is decreasing in the developed countries. The pediatric age is very important in terms of hearing and therefore speech development.
Uju Matilda Ibekwe   +1 more
doaj   +1 more source

Prevalence of Hearing Loss in Dutch Newborns; Results of the Nationwide Well-Baby Newborn Hearing Screening Program

open access: yesApplied Sciences, 2022
Background: Few studies report prevalence rates of hearing loss in newborns for nationwide populations. The Dutch well-baby newborn hearing screening covers almost all eligible children and has high participation rates for follow-up screening rounds and ...
Rosanne B. van der Zee   +3 more
doaj   +1 more source

The audiological phenotype of patients with a variant in MYH9 and MYH14 genes

open access: yesScientific Reports
Mutations in MYH9 and MYH14 are associated with autosomal dominant, progressive sensorineural hearing loss. This study aimed to characterize and compare the clinical and audiological features of patients with MYH9 or MYH14 variants.
Seong Hoon Bae   +7 more
doaj   +1 more source

Auditory genotype-phenotype correlation of patients with variants in STRC

open access: yesScientific Reports
Pathogenic variants in the STRC gene are among the most common causes of autosomal recessive non-syndromic hearing loss, particularly in cases with mild-to-moderate sensorineural hearing loss (SNHL).
Tae Uk Cheon   +6 more
doaj   +1 more source

Recent preclinical and clinical advances in gene therapy for hereditary hearing loss

open access: yesMolecules and Cells
: Hereditary hearing loss is a genetically heterogeneous condition that affects millions of people worldwide and has limited curative treatment options.
Seung Hyun Jang   +3 more
doaj   +1 more source

Biallelic variants of SEMA3F are associated with nonsyndromic hearing loss

open access: yesMolecules and Cells
: It is crucial to manage hearing loss and its associated public health impacts. In this study, we aimed to understand the role of Sema3f in the development and maintenance of the auditory system. Inner ear-specific Sema3f knockout mice exhibited hearing
Sun Young Joo   +11 more
doaj   +1 more source

Risk factors for hearing loss in children: a systematic literature review and meta-analysis protocol

open access: yesSystematic Reviews, 2019
Background Hearing loss in newborns and children is a public health concern, due to high prevalence and negative effects on their development. Early detection and intervention of childhood hearing loss may mitigate these negative effects.
Bénédicte Vos   +4 more
doaj   +1 more source

Roles of supporting cells in the maintenance and regeneration of the damaged inner ear: A literature review

open access: yesJournal of Otology
The inner ear sensory epithelium consists of two major types of cells: hair cells (HCs) and supporting cells (SCs). Critical functions of HCs in the perception of mechanical stimulation and mechanosensory transduction have long been elucidated.
Jing-Ying Guo   +3 more
doaj   +1 more source

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