DETECTION OF THE GJB2 MUTATION IN IRANIAN
CHILDREN WITH HEARING LOSS TREATED
WITH COCHLEAR IMPLANTATION
Peyvandi AA1, Morovvati S2,*, Rabiee HR3,
Ranjbar R3, Ajalloueyan M 4, Hassanalifard M4
*Corresponding Author: Saeid Morovvati, Research Center for Human Genetics, Baqiyatallah University of
Medical Sciences, Tehran, POB: 19395/5487, Iran; Tel./Fax: +98-21-88620812; E-mail: morovvati@hotmail.
com; morovvati@bmsu.ac.ir
page: 19
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CONCLUSIONS
The results of our study showed that CI is a suitable
choice for treatment of children with non syndromic
deafness, especially with mutations in the GJB2
gene. Mutation screening for deafness-causing mutations
in the GJB2 gene is a useful predictor of postimplantation
speech perception and permits better
pre-implantation counseling. We suggest microarray
or other advanced mutation detection methods for assessment
of other genes which might be responsible
for non syndromic deafness.
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