Loading…

Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey

Considerable differences on the frequencies of the mitochondrial 12S rRNA A1555G and tRNA(Ser(UCN)) A7445G mutations have been reported in different populations. Our screening of 168 patients coming from independent Turkish families with prelingual sensorineural non-syndromic deafness revealed three...

Full description

Saved in:
Bibliographic Details
Published in:European journal of pediatrics 2003-03, Vol.162 (3), p.154-158
Main Authors: TEKIN, M, DUMAN, T, BOGOCLU, G, INCESULU, A, COMAK, E, FITOZ, S, YILMAZ, E, IIHAN, I, AKAR, N
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Considerable differences on the frequencies of the mitochondrial 12S rRNA A1555G and tRNA(Ser(UCN)) A7445G mutations have been reported in different populations. Our screening of 168 patients coming from independent Turkish families with prelingual sensorineural non-syndromic deafness revealed three deaf children with A1555G (1.8%) but no examples of A7445G. One proband with the mitochondrial A1555G mutation has also evidence for right parietal infarct on a brain imaging study, for which common thrombotic mutations were found to be negative. This study shows that the mitochondrial A1555G mutation is among the significant causes of prelingual non-syndromic deafness in the Turkish population.
ISSN:0340-6199
1432-1076
DOI:10.1007/s00431-002-1129-z