نتایج جستجو برای: hereditary deafness

تعداد نتایج: 91403  

Journal: :iranian journal of public health 0
samira asgharzade somayeh reiisi mohammad amin tabatabaiefar morteza hashemzadeh chaleshtori

background: hearing loss (hl) is the most frequent neurosensory impairment. hl is highly heterogeneous defect. this disorder affects 1 out of 500 newborns. this study aimed to determine the role of dfnb2 locus and frequency of myo7a gene mutations in a population from west of iran. methods: thirty families investigated in shahrekord university of medical sciences in 2014, genetic linkage analys...

Journal: :iranian rehabilitation journal 0
mohammad rostami university of social welfare and rehabilitation sciences, tehran, iran. b bahmani university of social welfare and rehabilitation sciences, tehran, iran. vahid bakhtyari university of social welfare and rehabilitation sciences, tehran, iran. guita movallali university of social welfare and rehabilitation sciences, tehran, iran.

deafness is a heterogeneous condition with far-reaching effects on social, emotional, and cognitive development. many regard themselves as members of a cultural minority who use sign language. they should not continue to be neglected in research on depression. the purpose of this article is to investigate depression among the deaf people based on researches results. we identified relevant studi...

Journal: :Journal of veterinary internal medicine 2009
D Cvejic T A Steinberg M S Kent A Fischer

BACKGROUND Congenital sensorineural deafness has been reported frequently in experimental mixed-breed white cats but there is a paucity of data on occurrence of deafness in client-owned pure-breed white cats. OBJECTIVE To describe hearing status in client-owned pure-breed white cats. ANIMALS Eighty-four pure-breed client-owned cats with white coat color of 10 registered breeds presented for...

Journal: :Journal of medical genetics 2003
S Naz F Alasti A Mowjoodi S Riazuddin M H Sanati T B Friedman A J Griffith E R Wilcox

Genetic factors are thought to account for approximately one half of cases of childhood hearing loss, the majority of which is non-syndromic and not associated with other abnormalities. Seventy-seven percent of hereditary, non-syndromic, prelingual deafness is autosomal recessive, 22% is autosomal dominant, and 1% is transmitted as a matrilineal or X linked trait. So far, more than 30 distinct ...

2013
Tao Yang Xiaoming Wei Yongchuan Chai Lei Li Hao Wu

BACKGROUND Although over 60 non-syndromic deafness genes have been identified to date, the etiologic contribution of most deafness genes remained elusive. In this study, we addressed this issue by targeted next-generation sequencing of a large cohort of non-syndromic deaf probands. METHODS Probands with mutations in commonly screened deafness genes GJB2, SLC26A4 and MT-RNR1 were pre-excluded ...

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...

Journal: :Human molecular genetics 1998
V Kalatzis C Petit

What would define real progress in the field of deafness research in fundamental and medical terms? In fundamental terms, progress would be measured by an improvement in our knowledge of the development and physiology of the ear. In medical terms, progress would lead to the division of the broad category of hearing defects into distinct clinical entities or subclasses, the collection of epidemi...

2016
Shin-Ya Nishio Isabelle Schrauwen Hideaki Moteki Hela Azaiez

Copyright © 2016 Shin-ya Nishio et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Congenital sensorineural hearing loss is the most common sensory disorder, with approximately 1 in every 1000 newborns in developed countries s...

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