Literature DB >> 18654889

An unusually frequent beta-thalassemia mutation in an Iranian Province.

Peyman Eshghi1, Azita Zadeh-Vakili, Armin Rashidi, Ebrahim Miri-Moghaddam, Ebrahim Miri-Moghadam.   

Abstract

Iran, a country located on the "thalassemia belt", is an area with an unusually high prevalence of beta-thalassemia (thal). The gene frequency of thalassemia shows great variation within Iran from one area to another. The purpose of this study was to determine the spectrum of beta-thal mutations in Sistan-Baluchestan (S-B), a southeastern province of Iran which has a high mutation frequency of about 10%, and to compare this with neighboring provinces and countries. A total of 400 carriers (200 pre-marriage young couples selected at centers conducting prenatal diagnosis programs) with an established diagnosis of beta-thal minor, were enrolled into the study. Mutations in the beta-globin gene were detected using amplification refractory mutation system (ARMS) and restriction fraction length polymorphism (RFLP). Three hundred and sixty mutant chromosomes (13 different mutations) were detected with the two most common mutations accounting for about 80% of all detected beta-thal alleles in this region. The most common mutation by far was IVS-I-5 (G>C) (72.3%), followed by frameshift codons (FSC) 8/9 (+G) (5.8%) and codon 44 (-C) (2.5%). In conclusion, IVS-I-5 and FSC 8/9 (+G) account for about 80% of all mutations in S-B. Sistan-Baluchestan may be regarded as the 'hot zone' for the IVS-I-5 mutation.

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Year:  2008        PMID: 18654889     DOI: 10.1080/03630260701758932

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  4 in total

1.  A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka.

Authors:  M L Black; S Sinha; S Agarwal; R Colah; R Das; M Bellgard; A H Bittles
Journal:  J Community Genet       Date:  2010-10-10

2.  Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques.

Authors:  Zohreh Rahimi; Adriana Muniz; Abbas Parsian
Journal:  Mol Biol Rep       Date:  2009-05-13       Impact factor: 2.316

3.  Coincidence of Niemann-Pick Disease and beta-Thalassemia; a Case Report.

Authors:  Fatemeh Farahmand; Vajiheh Modaresi; Mina Izadyar; Fatemeh Mahjob
Journal:  Iran J Pediatr       Date:  2010-12       Impact factor: 0.364

4.  Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran.

Authors:  Ebrahim Miri-Moghaddam; Sara Bahrami; Majid Naderi; Ali Bazi; Morteza Karimipoor
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2017-04-01
  4 in total

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