نتایج جستجو برای: hereditary hearing loss

تعداد نتایج: 562756  

2015
Francesco Zonta Giorgia Girotto Damiano Buratto Giulia Crispino Anna Morgan Khalid Abdulhadi Moza Alkowari Ramin Badii Paolo Gasparini Fabio Mammano

Mutations in the GJB2 gene, which encodes the gap junction protein connexin 26 (Cx26), are the primary cause of hereditary prelingual hearing impairment. Here, the p.Cys169Tyr missense mutation of Cx26 (Cx26C169Y), previously classified as a polymorphism, has been identified as causative of severe hearing loss in two Qatari families. We have analyzed the effect of this mutation using a combinat...

Journal: :International Journal of Pediatric Otorhinolaryngology 2021

Hereditary non-syndromic hearing loss (NSHL) has a high genetic heterogeneity with about 152 genes identified as associated molecular causes. The present study aimed to detect the possible damaging variants of deaf probands from six unrelated Chinese families. After excluding pathogenic/likely pathogenic in most common genes, GJB2 and SLC26A4, 12 prelingual deafness autosomal recessive inherita...

Mutations in the connexin 26 (Cx26) gene at the DFNB1 locus on chromosome 13q12 are associated with autosomal recessive non-syndromic hearing loss (ARNSHL). There are many known mutations in this gene that cause hearing loss. A single frameshift, at position 35 (35delG) accounts for 50% of mutations in the Caucasian population with carrier frequencies of 1.5-2.5%. In this study we investigated ...

Background and purpose: Proper resonance is a major factor for the comprehension of speech in individuals with hearing loss. These people have low speech intelligibility caused by inappropriate resonance. Therefore, nasalance measurement is a principal aspect of the assessment of people with hearing loss. This study aimed at determining nasalance in children with hearing loss. Materials and me...

Journal: :International journal of clinical and experimental medicine 2015
Yue Huang Xiao-Lin Yang Wen-Xia Chen Bo Duan Ping Lu Yan Wang Zheng-Min Xu

GJB2 accounts for more than 80% of recessive forms of hereditary hearing loss (HL); however, the correlation between the p.V37I variant of GJB2 and hearing phenotype is controversial. This study aimed to investigate the clinical and epidemiological characteristics of the p.V37I variant in sensorineural hearing loss in Chinese infants (0-3 months). Hearing and gene tests were conducted in 300 in...

Farid Ataie, Mostafa Aflaki, Saeed Soheilipour,

  Hearing loss is a major social problem and its rehabilitation is very important. Considering its prevalence in Iran, this study was performed to evaluate cases of hearing loss in referrals of Alzahra and Edgehie audiometry centers during the years 1995-1996. The descriptive strategy of this study was carried out on referrals of two audiometry clinics in Isfahan from October 1995 to 1996. Ou...

Journal: :health scope 0
nazanin izadi center for research on occupational diseases, tehran university of medical sciences, tehran, ir iran mahdi sadeghi environmental health research center, golestan university of medical sciences, gorgan, ir iran; environmental health research center, golestan university of medical sciences, gorgan, ir iran. tel: +98-1732436102, fax: +98-1732436107 maryam saraie center for research on occupational diseases, tehran university of medical sciences, tehran, ir iran

conclusions due to the long exposure to the loud noise during the day, hearing loss in drivers is significant. the left ear displays greater loss than the right ear. therefore, strategies to prevent hearing loss in drivers could include education, lifestyle changes and compliance issues related to hearing health, use of personal protective equipment, conducting periodic examinations and early t...

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