مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

723
Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

MOLECULAR SPECTRUM OF β-THALASSEMIA MUTATIONS IN NORTHWESTERN IRAN

Pages

  33-36

Abstract

 Background and objective: b -Thalassemia is a hereditary autosomal disorder with decreased or absent b-globin chain synthesis. This study was designed to identify the common and rare b -thalassemia MUTATIONs in the Azerbaijan provinces, Northwestern Iran, and to set up a prenatal diagnostic laboratory.Materials and Methods: One hundred unrelated patients with known b-thalassemia major and intermedia, registered with the thalassemia clinics in provincial capitals of Tabriz and Ardebil, were examined. MUTATIONs were studied in 200 chromosomes, by Polymerase Chain Reaction-Amplification Refractory MUTATION System (PCR-ARMS) and direct Sequencing methods.Results: Seventeen different b- thalassemia MUTATIONs were found in this region of Iran. The results showed that IVS-II-1 (G®A) MUTATION was the most frequent, comprising 21% of all MUTATIONs. Other common MUTATIONs were IVS-I-110 (G®A) 18%, FSC-8/9 (+G) 14.5%, FSC-8 (-AA) 8% and IVS-I-1 (G®A) 7.5%. The other MUTATIONs were as follows; IVS-I-5 (G®C), FSC-44 (-C), Cd15 (TGG®TGA), FSC-5 (-CT), IVS-I-6 (T®C), IVS-II-848 (C®A), FSC- 36/37 (-T), -28 (A®C), FSC-25/26 (+T), IVS-II-745 (C®G), FSC-16 (-C) and IVS-I-25 (-25bp del). Overall these comprise 95% of b-thalassemia MUTATIONs in this region and 5% of the MUTATIONs still await exploration.Conclusion: The results of this study showed the similarities and differences between this region with the other regions of Iran and neighboring country This is the first comprehensive study in this region and could be useful for developing b-thalassemia molecular screening plan in Azerbaijan-Iran.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    HOSSEINPOUR FEYZI, M.A., HOSSEINPOUR FEYZI, A.A., POULADI, N., HAGHI, M., & AZARFAM, P.. (2009). MOLECULAR SPECTRUM OF β-THALASSEMIA MUTATIONS IN NORTHWESTERN IRAN. MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, 30(4), 33-36. SID. https://sid.ir/paper/47470/en

    Vancouver: Copy

    HOSSEINPOUR FEYZI M.A., HOSSEINPOUR FEYZI A.A., POULADI N., HAGHI M., AZARFAM P.. MOLECULAR SPECTRUM OF β-THALASSEMIA MUTATIONS IN NORTHWESTERN IRAN. MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2009;30(4):33-36. Available from: https://sid.ir/paper/47470/en

    IEEE: Copy

    M.A. HOSSEINPOUR FEYZI, A.A. HOSSEINPOUR FEYZI, N. POULADI, M. HAGHI, and P. AZARFAM, “MOLECULAR SPECTRUM OF β-THALASSEMIA MUTATIONS IN NORTHWESTERN IRAN,” MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, vol. 30, no. 4, pp. 33–36, 2009, [Online]. Available: https://sid.ir/paper/47470/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top