Hereditary Deafness Newsletter
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مقایسه سطح ادراک شنیداری و وضوح کلامی بعد از کاشت حلزون در بیماران پرهلینگوال مبتلا به کمشنوایی عمیقی ارثی و غیرارثی مراجعه کننده به بیمارستان حضرت رسول اکرم(ص)
Background & Aim: When inner ear is disturbed, both hearing sensitivity and selective property decrease. Early rehabilitation for proper progression of speech and language appropriate to age is mandatory. Several studies were performed to compare factors that affect the results of cochlear implantations to select the best candidates on the basis of different criteria. This study was underta...
متن کاملMutation Analysis of Connexin 26 Gene and Del (GJB6-D13S1830) in Patients with Hereditary Deafness from Two Provinces in Iran
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 ...
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