نتایج جستجو برای: congenital snhl

تعداد نتایج: 120665  

2017
Akira Yamaguchi Tsutomu Oh-ishi Takashi Arai Hideaki Sakata Nodoka Adachi Satoshi Asanuma Eiji Oguma Hirofumi Kimoto Jiro Matsumoto Hidetoshi Fujita Tadashi Uesato Jutaro Fujita Ken Shirato Hideki Ohno Takako Kizaki

OBJECTIVE Approximately 8-10% of newborns with asymptomatic congenital cytomegalovirus (cCMV) infection develop sensorineural hearing loss (SNHL). However, the relationship between CMV load, SNHL and central nervous system (CNS) damage in cCMV infection remains unclear. This study aimed to examine the relationship between urinary CMV load, SNHL and CNS damage in newborns with cCMV infection. ...

2015
Senthil Vadivu Arumugam Vijaya Krishnan Paramasivan Sathiya Murali Kiran Natarajan Sudhamaheswari Mohan Kameswaran

BACKGROUND The estimated prevalence of Sensory Neural Hearing Loss (SNHL) in patients less than 18 years of age is 6 per 1000. Roughly 50% of cases of congenital SNHL can be linked to a genetic cause, with approximately 30% being syndromic and the remaining 70% being non-syndromic. The term "syndromic" implies the presence of other distinctive clinical features in addition to hearing loss. The ...

Journal: :Pediatrics 2006
Ina Foulon Anne Naessens Walter Foulon Ann Casteels Frans Gordts

OBJECTIVE To determine the incidence, characteristics, and evolution of sensorineural hearing loss (SNHL) in infants with a congenital cytomegalovirus infection (cCMV). STUDY DESIGN In a prospective 10-year study, 14 021 unselected live-born infants were screened for cCMV by virus isolation in urine. Congenitally infected newborns were evaluated for SNHL during the first 5 years of life. RE...

Journal: :Turkish journal of medical sciences 2016
Mehmet Talay Köylü Gökçen Gökçe Güngor Sobaci Fahrettin Güven Oysul Dorukcan Akincioğlu

BACKGROUND/AIM The high prevalence of ophthalmologic pathologies in hearing-disabled subjects necessitates early screening of other sensory deficits, especially visual function. The aim of this study is to determine the frequency and clinical characteristics of ophthalmic pathologies in patients with congenital bilateral sensorineural hearing loss (SNHL). MATERIALS AND METHODS This descriptiv...

2014
Swetha G. Pinninti Mackenzie Dreher Karen Fowler Zdenek Novak William J. Britt Suresh Boppana Shannon Ross

Background. Congenital CMV (cCMV) is the leading non-genetic cause of sensorineural hearing loss (SNHL) in the U.S. Approximately 40-60% of infants with symptomatic cCMV infection develop long term sequelae such as hearing loss. Currently, there are no identified predictors of hearing loss. The objectiveis to determine clinical predictors of SNHL in infants with symptomatic cCMV infection. Meth...

2017
Juan C Falcón González Cándido Corujo-Santana Silvia A Borkoski-Barreiro Ángel Ramos

Permanent hearing loss in childhood is an important public health problem. Its prevalence, when considering only bilateral profund congenital sensorineural hearing loss (SNHL), is 1 in 1000 living newborns and 5 in 1000 when all degrees of hearing loss are considered [1]. Hearing loss produces not only permanent effects on oral language development but may also have implications in emotional an...

2013
Liliana Gabrielli Maria Paola Bonasoni Donatella Santini Giulia Piccirilli Angela Chiereghin Brunella Guerra Maria Paola Landini Maria Grazia Capretti Marcello Lanari Tiziana Lazzarotto

BACKGROUND Congenital cytomegalovirus (CMV) infection is a leading cause of sensorineural hearing loss (SNHL). The mechanisms of pathogenesis of CMV-related SNHL are still unclear. The aim is to study congenital CMV-related damage in the fetal inner ear, in order to better understand the underlying pathophysiology behind CMV-SNHL. RESULTS We studied inner ears and brains of 20 human fetuses, ...

Journal: :Archives of otolaryngology--head & neck surgery 1997
H Marres M van Ewijk P Huygen H Kunst G van Camp P Coucke P Willems C Cremers

OBJECTIVE To study nonsyndromic progressive sensorineural hearing loss (SNHL) with significant linkage to the DFNA2 locus on chromosome 1p in a Dutch kindred. DESIGN A 6-generation family with 194 family members was studied. Of the presumably affected persons, 43 were examined in detail to obtain audiograms and 37 underwent vestibulo-ocular examination. RESULTS Regression analysis showed si...

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