کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4112527 | 1606038 | 2011 | 4 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Association of GJB2 gene mutation with cochlear implant performance in genetic non-syndromic hearing loss
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موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
بیماری های گوش و جراحی پلاستیک صورت
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چکیده انگلیسی
ObjectiveTo analyze the association of GJB2 gene mutations with cochlear implant performance in children.MethodsSixty-five consecutive children who underwent cochlear implantation due to congenital profound senseurineural hearing between 2006 and 2008 were included in the study. In children, GJB2 gene mutation analysis was performed. Their auditory performance was assessed using MAIS, MUSS and LittlEARS tests.ResultsTwenty-two of sixty-five patients GJB2 mutations, and 35delG was the most frequent mutation. No significant difference was found between the auditory performance of mutation positive and negative children after one year follow up (p > 0.05).ConclusionGJB2 gene mutations do not impact on the outcome of cochlear implantation.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Pediatric Otorhinolaryngology - Volume 75, Issue 12, December 2011, Pages 1572–1575
Journal: International Journal of Pediatric Otorhinolaryngology - Volume 75, Issue 12, December 2011, Pages 1572–1575
نویسندگان
Recep Karamert, Yildirim A. Bayazit, Senay Altinyay, Akın Yılmaz, Adnan Menevse, Ozan Gokdogan, Cagil Gokdogan, Ayca Ant,