Williams syndrome is a neurodevelopmental disorder associated with cardiovascular problems, facial abnormalities and several behavioural and neurological disabilities. It is also characterized by some typical audiological features including abnormal sensitivity to sounds, cochlear impairment related to the outer hair cells of the basal turn of the cochlea, and sensorineural or mixed hearing loss, predominantly in the high frequency range. The aim of this report is to describe a follow-up study of auditory function in a cohort of children affected by this syndrome. 24 patients, aged 5\u201314 years, were tested by means of air/bone conduction pure-tone audiometry, immittance test and transient evoked otoacoustic emissions. They were evaluate...
BACKGROUND: Williams syndrome (WS) is a neurodevelopmental disorder characterized by hypersociabilit...
Objective: Recent reports have suggested a significant incidence of sensorineural hearing loss (SNHL...
Individuals with Williams syndrome (WS) have been shown to have atypical morphology in the auditory ...
The aim of this study was to investigate, in a clinical setting, the auditory function of a group of...
Objective: To assess if young subjects affected by Williams syndrome (WS) with normal middle ear fun...
Abstract—Background: Hyperacusis and phonophobia are common, debilitating symptoms in Williams syndr...
The aim of this study was to investigate the functionality of cochlear active mechanisms in normal-h...
Williams or Williams -Beuren Syndrome (WS) is a very rare syndrome associated with a microdeletion o...
Introduction: Williams syndrome (WS) is a rare neurodevelopment genetic condition. The syndrome may ...
Background: Williams syndrome (WS), a neurodevelopmental disorder, is characterized by pervasive cog...
Background  Williams Syndrome (WS) is a neurodevelopmental disorder of genetic origin, characteris...
This study examines the developmental history of 32 Williams syndrome patients, positive to the fluo...
Williams syndrome (WS), a genetic, neurodevelopmental disorder, is of keen interest to music cogniti...
Williams Syndrome (WS), a neurodevelopmental genetic disorder, is characterized by peaks and valleys...
RESUMEN: Objetivos: El objetivo de este estudio es verificar la existencia de una relación entre la ...
BACKGROUND: Williams syndrome (WS) is a neurodevelopmental disorder characterized by hypersociabilit...
Objective: Recent reports have suggested a significant incidence of sensorineural hearing loss (SNHL...
Individuals with Williams syndrome (WS) have been shown to have atypical morphology in the auditory ...
The aim of this study was to investigate, in a clinical setting, the auditory function of a group of...
Objective: To assess if young subjects affected by Williams syndrome (WS) with normal middle ear fun...
Abstract—Background: Hyperacusis and phonophobia are common, debilitating symptoms in Williams syndr...
The aim of this study was to investigate the functionality of cochlear active mechanisms in normal-h...
Williams or Williams -Beuren Syndrome (WS) is a very rare syndrome associated with a microdeletion o...
Introduction: Williams syndrome (WS) is a rare neurodevelopment genetic condition. The syndrome may ...
Background: Williams syndrome (WS), a neurodevelopmental disorder, is characterized by pervasive cog...
Background  Williams Syndrome (WS) is a neurodevelopmental disorder of genetic origin, characteris...
This study examines the developmental history of 32 Williams syndrome patients, positive to the fluo...
Williams syndrome (WS), a genetic, neurodevelopmental disorder, is of keen interest to music cogniti...
Williams Syndrome (WS), a neurodevelopmental genetic disorder, is characterized by peaks and valleys...
RESUMEN: Objetivos: El objetivo de este estudio es verificar la existencia de una relación entre la ...
BACKGROUND: Williams syndrome (WS) is a neurodevelopmental disorder characterized by hypersociabilit...
Objective: Recent reports have suggested a significant incidence of sensorineural hearing loss (SNHL...
Individuals with Williams syndrome (WS) have been shown to have atypical morphology in the auditory ...