نتایج جستجو برای: large vestibular aqueduct

تعداد نتایج: 1043675  

2011
Ying-Chang Lu Chen-Chi Wu Wen-Sheng Shen Ting-Hua Yang Te-Huei Yeh Pei-Jer Chen I-Shing Yu Shu-Wha Lin Jau-Min Wong Qing Chang Xi Lin Chuan-Jen Hsu

Recessive mutations in the SLC26A4 gene are a common cause of hereditary hearing impairment worldwide. Previous studies have demonstrated that different SLC26A4 mutations may have different pathogenetic mechanisms. In the present study, we established a knock-in mouse model (i.e., Slc26a4(tm1Dontuh/tm1Dontuh) mice) homozygous for the c.919-2A>G mutation, which is a common mutation in East Asian...

2016
A.C. Gonçalves R. Santos A. O'Neill P. Escada G. Fialho H. Caria

Pendred syndrome (PS) is the second most common type of autosomal recessive syndromic hearing loss (HL). It is characterised by sensorineural HL and goiter with occasional hypothyroidism. These features are generally accompanied by malformations of the inner ear, as enlarged vestibular aqueduct (EVA). In about 50% of probands, mutations in the SLC26A4 gene are the cause of the disease. Here we ...

Journal: :The Laryngoscope 2014
Yasuhide Okamoto Hideki Mutai Atsuko Nakano Yukiko Arimoto Tomoko Sugiuchi Sawako Masuda Noriko Morimoto Hirokazu Sakamoto Noboru Ogahara Akira Takagi Hidenobu Taiji Kimitaka Kaga Kaoru Ogawa Tatsuo Matsunaga

OBJECTIVES/HYPOTHESIS To investigate possible association of hearing loss and SLC26A4 mutations with the subgroups of enlarged vestibular aqueduct (EVA) morphology in Japanese subjects with hearing loss. STUDY DESIGN Retrospective multicenter study. METHODS Forty-seven subjects who had vestibular aqueduct with midpoint diameter >1 mm by computed tomography of the temporal bone were enrolled...

2016
Hong Wu Yong Feng Lu Jiang Qian Pan Yalan Liu Chang Liu Chufeng He Hongsheng Chen Xueming Liu Chang Hu Yiqiao Hu Lingyun Mei

OBJECTIVE The aim of this study was to evaluate the GoldenGate microarray as a diagnostic tool and to elucidate the contribution of the genes on this array to the development of both nonsyndromic and syndromic sensorineural hearing loss in China. METHODS We developed a microarray to detect 240 mutations underlying syndromic and nonsyndromic sensorineural hearing loss. The microarray was then ...

2018
Sebastian Roesch Emanuele Bernardinelli Charity Nofziger Miklós Tóth Wolfgang Patsch Gerd Rasp Markus Paulmichl Silvia Dossena

The prevalence and spectrum of sequence alterations in the SLC26A4 gene, which codes for the anion exchanger pendrin, are population-specific and account for at least 50% of cases of non-syndromic hearing loss associated with an enlarged vestibular aqueduct. A cohort of nineteen patients from Austria with hearing loss and a radiological alteration of the vestibular aqueduct underwent Sanger seq...

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