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Vestn Otorinolaringol ; (2): 17-9, 2009.
Article in Russian | MEDLINE | ID: mdl-19491791

ABSTRACT

This paper reports the first case of cochlear implantation performed in this country in a child with congenital non-syndromic sensorineural loss of hearing having hereditary etiology and attributable to autosomal-recessive 35 delG mutation in locus DFNB1 (13q.11-q12) of GJB2 (connexin 26) gene.


Subject(s)
Cochlear Implantation/methods , Connexins/genetics , DNA/genetics , Genetic Predisposition to Disease , Hearing Loss, Sensorineural/surgery , Mutation , Child, Preschool , Connexin 26 , DNA Mutational Analysis , Hearing Loss, Sensorineural/congenital , Hearing Loss, Sensorineural/genetics , Humans , Male , Pedigree
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