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:

2,655
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:

1

Information Journal Paper

Title

PARENTAL LABORATORY FINDINGS OF PATIENTS WITH HOMOZYGOUS THALASSEMIA REFERRED TO IMMAM HOSSEIN HOSPITAL(1998)

Pages

  81-88

Keywords

Not Registered.

Abstract

 History and Objectives: Due to the prevalence of the beta-thalassemia carriership in our country, and the emphasis on the controlling and prophylaxis of the chronic symptoms, we decieded to review complete blood count (CBe) and hemoglobin electrophoresis among parents of major beta thalassemic patients that were referred to the Immam Hossein Hospital in 1997-1998. Materials and Methods: A descriptive study concerning parents of all beta-thalassemic patients that are referred to the Imam Hossein Hospital was carried out. Blood samples were taken for CBC and electrophoretic analysis. MCV and MCH levies of lower than 80fL and 27pg respectively were considered abnormal. HbA2levels higher than 3.5% was also considered as abnormal. Results: All 48 candidates (100%) had reduced MCV and MCR. MCV and MCH were 60I45fL and 20I1.5pg respectively. 62.5% had increased and 37.5% had normal RBC count. No record of low RBC was encountered. Results of electrophoretic test were as follows: HbF 2.4 I 2.4% and HbA2 5.2I1.1%. 89.5% of individuals had abnormal electrophoretic results and 10.5% had normal HbA2 levels (lower than 3.5%). Conclusions: All parents of beta-thalessemic major patients had abnormality in their CBC index, therefore the first step in evaluation of beta-thalassemia ought to be CBC assessment and once abnormal results are reported then electrophoretic analysis should be carried out. Further study on the diagnostic efficiency of CBC index in detection of minor beta-thalassemia is recommended.  

Cites

References

  • No record.
  • Cite

    APA: Copy

    EHTERAM, H., & SHAFAGHI, B.. (2000). PARENTAL LABORATORY FINDINGS OF PATIENTS WITH HOMOZYGOUS THALASSEMIA REFERRED TO IMMAM HOSSEIN HOSPITAL(1998) . FEYZ, 4(13), 81-88. SID. https://sid.ir/paper/370758/en

    Vancouver: Copy

    EHTERAM H., SHAFAGHI B.. PARENTAL LABORATORY FINDINGS OF PATIENTS WITH HOMOZYGOUS THALASSEMIA REFERRED TO IMMAM HOSSEIN HOSPITAL(1998) . FEYZ[Internet]. 2000;4(13):81-88. Available from: https://sid.ir/paper/370758/en

    IEEE: Copy

    H. EHTERAM, and B. SHAFAGHI, “PARENTAL LABORATORY FINDINGS OF PATIENTS WITH HOMOZYGOUS THALASSEMIA REFERRED TO IMMAM HOSSEIN HOSPITAL(1998) ,” FEYZ, vol. 4, no. 13, pp. 81–88, 2000, [Online]. Available: https://sid.ir/paper/370758/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top