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 …
cause of congenital sensorineural hearing loss and is frequently progressive. Imaging is …
Syndromic hearing loss in children
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 …
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 …
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 …
While a strong correlative relationship between EVA and hearing loss is well established, its …
Vestibular manifestations in subjects with enlarged vestibular aqueduct
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 …
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 …
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 …
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 …
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 …
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 …
SLC26A4 mutations: congenital, fluctuating, and progressive hearing loss usually …