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Central Library of Kurdistan University of Medical Sciences
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:: Volume 19, Issue 1 (Scientific Journal of Kurdistan University of Medical Sciences 2014) ::
SJKU 2014, 19(1): 58-66 Back to browse issues page
The frequency of the most common Mediterranean mutation in phenylketonuria patients in Kermanshah Province
Kayvan Moradi1 , Reza Alibakhshi 2, Kamran Alimadadi3
1- Shahid Chamran University of Ahvaz
2- Kermanshah University of Medical Sciences , ralibakhshi@kums.ac.ir
3- State Welfare Organization of Kermanshah Province
Abstract:   (8196 Views)
Background and Aim: Phenylketonuria (PKU) is one of the major causes of mental retardation which is caused by mutations in the phenylalanine hydroxylase (PAH) gene. Early diagnosis and timely treatment can prevent the complications of this disorder. IVS10-11G>A mutation in (PAH) gene, has been known as the major mutation in Iran, Mediterranean region and Southern Europe. The aim of this study was to determine the frequency of IVS10-11G>A mutation in Kurdish patients with PKUin Kermanshah Province and compare it with the frequencies found in the studies in other parts of Iran. Material and Methods: From 2010 to 2011, we identified 27 unrelated families with classical PKU from different parts of Kermanshah Province. The DNA fragments containing the exon 11 of the PAH gene and its flanking intronic sequences were amplified and sequenced. Results: The frequency of IVS10-11G>A mutation was 7.4% which was found in two homozygous PKU patients. These patients had classic PKU phenotype and their parents were 4th degree relatives. Conclusion: The findings of this study supported the results of our previous study. It seems that there is a distinct difference in PAH characters of mutations between Kermanshah and the other parts of Iran. Therefore, study of the PAH gene mutations in other parts of Iran and use of these studies for future plans, including screening of carriers are recommended. Received: Jul 2, 2013 Accepted: Dec 11, 2013 Conflict of interest: None declared
Keywords: Kermanshah, Phenylketonuria, Mediterranean mutation
Full-Text [PDF 264 kb]   (2836 Downloads)    
Type of Study: Original Research | Subject: General
Received: 2014/03/16 | Accepted: 2014/03/16 | Published: 2014/03/16
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Moradi K, Alibakhshi R, Alimadadi K. The frequency of the most common Mediterranean mutation in phenylketonuria patients in Kermanshah Province. SJKU 2014; 19 (1) :58-66
URL: http://sjku.muk.ac.ir/article-1-1278-en.html


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Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 19, Issue 1 (Scientific Journal of Kurdistan University of Medical Sciences 2014) Back to browse issues page
مجله علمی دانشگاه علوم پزشکی کردستان Scientific Journal of Kurdistan University of Medical Sciences
مجله علمی دانشگاه علوم پزشکی کردستان Scientific Journal of Kurdistan University of Medical Sciences
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