Results 61 to 70 of about 179,610 (183)
Impact of the COVID‐19 Pandemic on Cochlear Implant Usage in Children
Abstract Objective To evaluate the impact of the COVID‐19 pandemic on cochlear implant (CI) usage in children by comparing hearing hour percentage (HHP) during the pandemic to prepandemic levels. Study Design Retrospective Cohort Study. Setting Primary Children's Hospital, Utah.
Peter Kfoury +7 more
wiley +1 more source
Superior semicircular canal dehiscence and enlarged vestibular aqueduct.
Superior semicircular canal dehiscence is a well described labyrinthine defect, detect in pediatric population too. We report a case of superior semicircular canal dehiscence, which radiological diagnosis was confirmed by multiplanar reformatted CT ...
BRANDOLINI, CRISTINA +3 more
core +1 more source
Purpose The assessment of endolymphatic hydrops (ELH) with specific MRI sequences underlines the ability to evaluate intralabyrinthine changes objectively and radiologically. The visualization of ELH by MRI allows correlations to be made with clinical patterns and supports the diagnosis of Ménière′s disease (MD).
Christoph J. Pfeiffer +6 more
wiley +1 more source
Cochlear implantation (CI) is a safe and well‐established intervention for sensorineural hearing loss, with a low incidence of severe postoperative infections. We present the first reported case of cerebellar abscess and herniation due to CI infection. This unique case involves a 57‐year‐old man with recurrent cochlear implant infections, necessitating
Celine Molfetta +5 more
wiley +1 more source
A Novel LMX1A Frameshift Variant Underlies Familial Phenotypic Heterogeneity in DFNA7
Pathogenic variants in the LIM‐homeodomain transcription factor LMX1A represent a rare yet critical etiology for autosomal dominant nonsyndromic hearing loss 7 (DFNA7) and less frequently, its autosomal recessive counterpart (ARNSHL). Here, we describe a novel heterozygous frameshift variant, LMX1A c.405delT (p.Phe135LeufsTer3), identified in a three ...
Chenyang Xu +6 more
wiley +1 more source
Review of the Molecular and Developmental Basis of Myhre Syndrome, Bench Research
ABSTRACT Myhre syndrome (MS) is a connective‐tissue disorder within the acromelic dysplasia spectrum. It is characterized by congenital craniofacial, skeletal, cutaneous anomalies, respiratory, cardiovascular along with intellectual disability, deafness, and progressive fibrosis.
Camille Viaut, Valerie Cormier‐Daire
wiley +1 more source
A 12-year-old girl with known bilateral enlarged vestibular aqueducts presented with vertigo and sudden profound hearing loss in her only hearing ear after COVID-19 infection.
Genevieve Min Lee +3 more
doaj +1 more source
International Pediatric Otolaryngology Group (IPOG) Consensus on Vestibular Testing in Children
This study represents the first international consensus on vestibular testing in children. Twenty‐one international experts from nine countries provided guidelines on the recommended minimum test battery necessary to perform a pediatric vestibular assessment.
A. Coudert +20 more
wiley +1 more source
Identification of the inner ear malformation types from radiographs is a complex process. We hypothesize that each inner ear anatomical type has a uniqueness in its appearance in radiographs.
Anandhan Dhanasingh +7 more
doaj +1 more source
Correlation of vestibular aqueduct size with air-bone gap in enlarged vestibular aqueduct syndrome.
OBJECTIVES/HYPOTHESIS: Patients with enlarged vestibular aqueduct (EVA) often demonstrate an air-bone gap (ABG) at low frequencies on audiometric testing. The mechanism for this has not been well elucidated.
김진아, 최재영
core +1 more source

