نتایج جستجو برای: neural hearing loss

تعداد نتایج: 771165  

Journal: :Practica Oto-Rhino-Laryngologica 1985

الهی, فاضل, مهدوی, محمدرضا, ساوج, شکوفه, نژادگشتی, حسین,

Fechtner syndrome is an autosomal dominant syndrome which is defined by cataract, sensory neural hearing loss, kidney involvement, macrothrombocytopenia and neutrophilic inclusion bodies. We report a 21-year-old man with a history of idiopathic thrombocytopenic purpura, cataract and hearing loss who was admitted for work up renal failure. His blood smear showed macrothrombocytopenia...

2013
Samira Anderson Travis White-Schwoch Hee Jae Choi Nina Kraus

Aging results in a loss of sensory function, and the effects of hearing impairment can be especially devastating due to reduced communication ability. Older adults with hearing loss report that speech, especially in noisy backgrounds, is uncomfortably loud yet unclear. Hearing loss results in an unbalanced neural representation of speech: the slowly-varying envelope is enhanced, dominating repr...

Introduction: It seems that diabetes mellitus (DM) can affect the auditory system due to neuropathy, micro-vascular complications, and hearing cell damage during hyperglycemic states. In the current study, we aimed to compare hearing status in patients with type 2 DM (T2DM) according to their blood-sugar control status.   Materials and Methods: This cross-sectional study was carried out in 104 ...

Ahadi, Mohsen, Asad Malayeri, Saeid, Atabaki Mehr, Sepideh, Jafari, Zahra,

Objectives: The aim of the present study was to investigate satisfaction levels with hearing aids in daily life of older adult users, in addition to associated factors. Methods & Materials: In this cross sectional study, 32 subjects with moderate to severe sensory neural hearing loss (mean age; 63.5±9.8 Yrs) and different socio-economic status, referred to private practice audiology clinic (...

Journal: :international journal of molecular and cellular medicine 0
majid fardaei department of medical genetics, shiraz university of medical sciences, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) shaghayegh sarrafzadeh department of medical genetics, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) soudeh ghafouri-fard department of medical genetics, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) mohammad miryounesi genomic research center, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

hearing loss (hl) is the most common sensory defect. various genetic as well as environmental factors have been shown to contribute in it. more than 100 loci have been recognized to cause autosomal recessive nonsyndromic hearing loss (arnshl). here, we report a 6-year old female patient with bilateral pre-lingual hl in whom a mutation has been identified in triobp gene (c.6362c>t, s2121l). in s...

Journal: :Archives of disease in childhood 1985
B C Bradford J Baudin M J Conway J W Hazell A L Stewart E O Reynolds

Brainstem auditory evoked potentials were recorded in 117 newborn infants of less than 33 weeks of gestation. The potentials were absent in 10 infants (bilaterally in eight and unilaterally in two) and present in 107. By 1 year of age nine of the 10 infants with absent brainstem auditory evoked potentials were shown to have sensory neural hearing loss and required hearing aids: the remaining in...

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