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

video

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

sound

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

Persian Version

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

View:

237
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

90
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Prevalence of Hemoglobin Mutations and Hemoglobinopathies in Masjed Soleiman County, Southeastern Iran

Author(s)

ASADI FATEMEH | Rasouli Ghahfarokhi Seyedeh Moloud | Talebi Forough | Issue Writer Certificate 

Pages

  48-54

Abstract

 Background and Objectives: Hemoglobinopathies are characterized by defects in the synthesis of globin chains of hemoglobin (Hb). The purpose of the present study was to evaluate mutations associated with thalassemia and other Hemoglobinopathies in Masjed Soleiman County, Iran. Methods: This descriptive study was carried out on 456 individuals suspected of having Hemoglobinopathies who were referred to health centers of the Masjed Soleiman Country in 2015-2017. Blood samples were collected in EDTA tubes. Complete blood count test was performed and red blood cell indices were determined. Level of HB variants was measured using capillary electrophoresis. Reverse dot-blot, gap-polymerase chain reaction and Sanger sequencing were carried out to detect mutations. Results: We found that 17. 7% of the subjects were heterozygous for β-Thalassemia. Frequency of mutations 36/37 (– T), IVS-II-1 (G>A) and IVS-I-110 (G>A) in the β-globin gene was 26. 7%, 22% and 16. 27%, respectively. In addition, 9. 5% of the subjects contained Hb S, Hb D and Hb C, while 1. 1% of the subjects showed co-inheritance of an HB variant and β-Thalassemia. In subjects with α-Thalassemia, the-α 3. 7 (57. 1%),--MED– (17. 4%),-α 4. 2 (3. 1%) and-α 20. 5 (1. 5%) deletions were found as the most prevalent mutations. Conclusion: In addition to the high prevalence of β-Thalassemia and HBB gene mutations, we detected variants Hb S, Hb D, Hb C and co-inheritance of an HB variants and β-Thalassemia in individuals living in the Masjed Soleiman Country. We also identified four mutations in the α-globin gene. These results can be useful for genetic counseling in this population.

Cites

  • No record.
  • References

    Cite

    APA: Copy

    ASADI, FATEMEH, Rasouli Ghahfarokhi, Seyedeh Moloud, & Talebi, Forough. (2019). Prevalence of Hemoglobin Mutations and Hemoglobinopathies in Masjed Soleiman County, Southeastern Iran. MEDICAL LABORATORY JOURNAL, 13(2), 48-54. SID. https://sid.ir/paper/719890/en

    Vancouver: Copy

    ASADI FATEMEH, Rasouli Ghahfarokhi Seyedeh Moloud, Talebi Forough. Prevalence of Hemoglobin Mutations and Hemoglobinopathies in Masjed Soleiman County, Southeastern Iran. MEDICAL LABORATORY JOURNAL[Internet]. 2019;13(2):48-54. Available from: https://sid.ir/paper/719890/en

    IEEE: Copy

    FATEMEH ASADI, Seyedeh Moloud Rasouli Ghahfarokhi, and Forough Talebi, “Prevalence of Hemoglobin Mutations and Hemoglobinopathies in Masjed Soleiman County, Southeastern Iran,” MEDICAL LABORATORY JOURNAL, vol. 13, no. 2, pp. 48–54, 2019, [Online]. Available: https://sid.ir/paper/719890/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button