Progressive hearing loss and head trauma in enlarged vestibular aqueduct: a systematic review and meta-analysis

AS Alemi, DK Chan - Otolaryngology--Head and Neck …, 2015 - journals.sagepub.com
Objective Enlarged vestibular aqueduct is the most common radiographically identified
cause of congenital sensorineural hearing loss and is frequently progressive. Imaging is …

Syndromic hearing loss in children

M Lewis, CD Robson, DA Felice - Neuroimaging …, 2023 - neuroimaging.theclinics.com
The estimated prevalence of permanent bilateral hearing loss (HL) in children is 1.33 per
1000 live births, increasing to 3.5 per 1000 adolescents, presumably reflecting additional …

SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct

KA King, BY Choi, C Zalewski, AC Madeo… - The …, 2010 - Wiley Online Library
Abstract Objectives/Hypothesis: Identify correlations among SLC26A4 genotype, cochlear
structural anomalies, and hearing loss associated with enlargement of the vestibular …

Vestibular dysfunction in patients with enlarged vestibular aqueduct

CK Zalewski, WW Chien, KA King… - … –Head and Neck …, 2015 - journals.sagepub.com
Objective Enlarged vestibular aqueduct (EVA) is the most common inner ear malformation.
While a strong correlative relationship between EVA and hearing loss is well established, its …

Vestibular manifestations in subjects with enlarged vestibular aqueduct

JJ Song, SK Hong, SY Lee, SJ Park, SI Kang… - Otology & …, 2018 - journals.lww.com
Objective: To describe the results of a thorough evaluation in a large series of patients with
an enlarged vestibular aqueduct (EVA), focusing on vestibular manifestations with …

Systematic review on vestibular symptoms in patients with enlarged vestibular aqueducts

MC Stahl, T Otteson - The Laryngoscope, 2022 - Wiley Online Library
Objective Enlarged vestibular aqueduct (EVA) is a congenital condition that can lead to
various outcomes in pediatric patients including hearing loss and vestibular dysfunction. Our …

Establishment of a Knock-In Mouse Model with the SLC26A4 c.919-2A>G Mutation and Characterization of Its Pathology

YC Lu, CC Wu, WS Shen, TH Yang, TH Yeh, PJ Chen… - PloS one, 2011 - journals.plos.org
Recessive mutations in the SLC26A4 gene are a common cause of hereditary hearing
impairment worldwide. Previous studies have demonstrated that different SLC26A4 …

[HTML][HTML] Mouse models for pendrin-associated loss of cochlear and vestibular function

P Wangemann - Cellular Physiology and Biochemistry, 2013 - karger.com
The human gene SLC26A4 and the mouse ortholog Slc26a4 code for the protein pendrin,
which is an anion exchanger expressed in apical membranes of selected epithelia. In the …

Vestibular symptoms in children with enlarged vestibular aqueduct anomaly

JF Grimmer, G Hedlund - International journal of pediatric …, 2007 - Elsevier
OBJECTIVE: The objective of this study is to describe the vestibular symptoms in pediatric
patients with enlarged vestibular aqueduct (EVA) anomaly. METHODS: Retrospective chart …

Clinical characteristics and genotype–phenotype correlation of hearing loss patients with SLC26A4 mutations

H Suzuki, A Oshima, K Tsukamoto, S Abe… - Acta oto …, 2007 - Taylor & Francis
Conclusions. The present study confirmed the clinical characteristics of patients with
SLC26A4 mutations: congenital, fluctuating, and progressive hearing loss usually …