نتایج جستجو برای: deafness

تعداد نتایج: 7684  

Journal: :International journal of surgery science 2022

In patients with diabetes mellitus, by the time hearing loss is detected using conventional tuning for ktests, damage has already affected sensorineural component, which will affect component of patient and hence quality life. Therefore audiometry early detection in people Type 2 Diabetes mellitus scan be done. It help us to take steps make aware deafness measures prevention further progression...

Journal: :iranian red crescent medical journal 0
tahereh soleimanieh naeini department of psychology and education of exceptional children, islamic azad university- central tehran branch, & pediatric neuro-rehabilitation research center, university of social welfare and rehabilitation sciences, tehran, ir iran farnaz keshavarzi arshadi department of clinical psychology, islamic azad university- central tehran branch, tehran, ir iran nikta hatamizadeh pediatric neuro-rehabilitation research center, university of social welfare and rehabilitation sciences, tehran, ir iran; corresponding author: nikta hatamizadeh, pediatric neuro-rehabilitation research center, university of social welfare and rehabilitation sciences, tehran, ir iran. tel: +98-2122180132, fax: +98-2122180132, e-mail: enayatollah bakhshi department of biostatistics, university of social welfare and rehabilitation sciences, tehran, ir iran

conclusions it is likely that learning social skills in adolescents with deafness would improve their sense of competence, and emotional well being. results the intervention led to significant improvement in total perceived competence scores of adolescents with deafness (p < 0.001) as well as in three domains of socio-emotional competence (p = 0.003), communication competence (p < 0.001), and s...

2016
Penghui Chen Longxia He Xiuhong Pang Xiaowen Wang Tao Yang Hao Wu

Nonsyndromic deafness is genetically heterogeneous but phenotypically similar among many cases. Though a variety of targeted next-generation sequencing (NGS) panels has been recently developed to facilitate genetic screening of nonsyndromic deafness, some syndromic deafness genes outside the panels may lead to clinical phenotypes similar to nonsyndromic deafness. In this study, we performed com...

2014
Karin Lundin Fredrik Stillesjö Helge Rask-Andersen

Objective: The aim of the present study was to gauge factors that influence the outcome of cochlear implants (CI) in patients who have been deaf for an extended period. Patients and Methods: Twelve adult cases (13 ears) were operated on at the CI unit in Uppsala during the period of 2002–2013. These patients had a deafness duration ranging between 20 and 72 years in the implanted ear and severe...

Journal: :The Journal of speech and hearing disorders 1990
J F Knutson C R Lansing

Communication strategies, accommodations to deafness, and perceptions of the communication environment by profoundly deaf subjects were correlated with indices of psychosocial adjustment to determine whether accommodations to deafness could play a role in the presence of psychological difficulties among deaf persons. Persons with postlingually acquired profound deafness were administered the Co...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1986
A S Buchman D C Garron J E Trost-Cardamone M D Wichter M Schwartz

Since its original description the diagnosis of word deafness has been greatly expanded. Confusion has arisen with regard to the usage of the related terms pure word deafness, auditory agnosia, and cortical deafness. Three new cases of word deafness are presented including one case with CT and necropsy correlation. These cases are compared with 34 previously reported cases of various cortical a...

Journal: :BMJ 1965

Journal: :iranian journal of public health 0
&amp;quot;m hashemzadeh chaleshtori m dowlati dd farhud l hoghooghi rad r sasanfar a hoseinipour m montazer zohour

mutations in the gjb2 gene encoding connexin 26 (cx26) protein are a major cause for autosomal recessive non syndromic and sporadic deafness in many populations. in this study we have investigated the prevalence of the gjb2 gene mutations using nested pcr pre screening strategy and direct sequencing method. two hundred and sixty autosomal recessive non syndromic and sporadic deaf subjects from ...

2010
Susan Sommerlad Allan F. McRae Brenda McDonald Isobel Johnstone Leigh Cuttell Jennifer M. Seddon Caroline A. O'Leary

BACKGROUND Congenital sensorineural deafness is an inherited condition found in many dog breeds, including Australian Stumpy-tail Cattle Dogs (ASCD). This deafness is evident in young pups and may affect one ear (unilateral) or both ears (bilateral). The genetic locus/loci involved is unknown for all dog breeds. The aims of this study were to determine incidence, inheritance mechanism, and poss...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید