نتایج جستجو برای: syndromic sporadic hearing loss

تعداد نتایج: 510174  

Journal: :Brazilian journal of otorhinolaryngology 2007
Vânia Belintani Piatto Otávio Augusto Vasques Moreira Magali Aparecida Orate Menezes da Silva José Victor Maniglia Márcio Coimbra Pereira Edi Lúcia Sartorato

UNLABELLED Mutations in the connexin 26 gene seem to be extremely common in non-syndromic hereditary deafness genesis, especially the 35delG, but there are still only a few studies that describe the audiometric characteristics of patients with these mutations. AIM to analyze the audiometric characteristics of patients with mutations in the connexin 26 gene in order to outline genotype-phenoty...

2014
MINXING TAN XIAOFEI SHEN JUN YAO QINJUN WEI YAJIE LU XIN CAO GUANGQIAN XING

Hearing loss is the most common sensory deficit in humans and gaining a better understanding of the underlying causes is necessary to improve counseling and rehabilitation. In the present study, a genetic analysis of a Chinese family with autosomal dominant non‑syndromic progressive hearing impairment was conducted and assessed. Whole‑exome sequencing in combination with a co‑segregation analys...

ابهجی, مریم, اسمیت, ریچارد, بزاز زادگان, نیلوفر, جوان, محمد خلیل, خدایی, حسین, دهقانی, عاطفه, ریاض الحسینی, یاسر, سیفتی, مرتضی, مغنی باشی, مهدی, میراب, محمود, نجم آبادی, حسین, کهریزی, کیمیا,

Introduction: Hearing loss is the most common sensory neural defect in humans, affecting 1 in 1000 neonates, with over half of these cases predicted to be hereditary in nature. Most hereditary hearing loss is inherited in a recessive fashion, accounting for approximately 80 % of non-syndromic hearing loss (NSHL). Mutations in GJB2 gene are major cause of inherited deafness in the European an...

Journal: :Archives of disease in childhood 1983
M Vanderschueren-Lodeweyckx F Debruyne L Dooms E Eggermont R Eeckels

Hearing acuity was assessed in 45 children with sporadic congenital hypothyroidism during adequate long-term treatment. Otoscopy was performed in each and additional tympanometry in some of them. Secretory otitis media was found in 6 and was treated medically or by inserting grommets in the eardrum. In these children, hearing acuity was assessed after the otitis had been cured. Hearing acuity w...

آبسواران, ابوالفضل, اسماعیلی, محسن, جبارپور بنیادی, مرتضی, لطفلیزاده, نادر, یونس پور, رضا,

Background and Objective: Profound hearing loss is one of the most prevalent congenital disorders affecting about 1 in 1000 newborns. Autosomal recessive non-syndromic hearing loss (ARNSHL) is the predominant form of the severe inherited childhood deafness. This type of hearing loss in one-half of the cases is caused by mutations in GJB2 (connexin 26) and GJB6 (connexin 30) genes located at DFN...

Journal: :Journal of medical genetics 1999
G Van Camp H Kunst K Flothmann W McGuirt J Wauters H Marres M Verstreken I N Bespalova M Burmeister P H Van de Heyning R J Smith P J Willems C W Cremers M M Lesperance

Non-syndromic hearing impairment is one of the most heterogeneous hereditary conditions, with more than 40 reported gene localisations. We have identified a large Dutch family with autosomal dominant non-syndromic sensorineural hearing impairment. In most patients, the onset of hearing impairment is in the first or second decade of life, with a slow decline in the following decades, which stops...

Journal: :The journal of international advanced otology 2015
Sevcan Tuğ Bozdoğan Gökhan Kuran Özge Özalp Yüregir Hüseyin Aslan Süheyl Haytoğlu Akif Ayaz Osman Kürşat Arıkan

OBJECTIVE To date, studies in all populations showed that mutations in the gene of Gap junction protein beta 2 (GJB2) play an important role in non-syndromic autosomal recessive congenital hearing loss. The aim of this study was to evaluate GJB2 gene of patients with hearing loss in our region using deoxyribonucleic acid (DNA) sequencing method and to demonstrate region-specific mutation and po...

2011
Célia Nogueira Miguel Coutinho Cristina Pereira Alessandra Tessa Filippo M. Santorelli Laura Vilarinho

The understanding of the molecular genetics in sensorineural hearing loss (SNHL) has advanced rapidly during the last decade, but the molecular etiology of hearing impairment in the Portuguese population has not been investigated thoroughly. To provide appropriate genetic testing and counseling to families, we analyzed the whole mitochondrial genome in 95 unrelated children with SNHL (53 nonsyn...

2012
Jeong-In Baek Se-Kyung Oh Dong-Bin Kim Soo-Young Choi Un-Kyung Kim Kyu-Yup Lee Sang-Heun Lee

BACKGROUND Hereditary hearing loss is one of the most common heterogeneous disorders, and genetic variants that can cause hearing loss have been identified in over sixty genes. Most of these hearing loss genes have been detected using classical genetic methods, typically starting with linkage analysis in large families with hereditary hearing loss. However, these classical strategies are not we...

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