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:

211
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

104
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

QUANTITATIVE IMMUNOPHEMOTYPING OF PLATELET SURFACE GLYCOPROTEINS AMONG IRANIAN PATIENTS WITH BERNARD-SOULIER SYNDROME

Pages

  3-9

Abstract

 Background: Bernard-Soulier syndrome is a rare inherited BLEEDING disease caused by quantitative or qualitative defect of GPIb/IX/V, a platelet complex that binds the Von Willebrand factor. The expression of GPIB-IX-V complex can be evaluated by FLOW CYTOMETRY and confirmed by the absence of ristocetin-induced platelet aggregation in platelet-rich plasma. The main aim of the present study was to classify Iranian Bernard-Soulier syndrome patients by a flow cytometric method, and to evaluate the correlation between platelet immunophenotype and clinical findings among patients.Patients and Methods: The surface expression level of GPIB-IX-V on platelets was assessed in fifteen Bernard-Soulier syndrome patients, using a panel of antibodies using a quantitative FLOW CYTOMETRY method. The results of the physical examination, family history and clinical presentation were also recorded by a physician.Result: The present study showed that all the patients suffer from a severe form of GPIB-IX-V complex deficiency.The study also found no correlation between the platelet surface glycoprotein expression and severity of BLEEDING among patients.Conclusion: Severe quantitative defect is the most common subtype among Iranian patients with Bernard-Soulier syndrome. Platelet Immunophenotyping alone does not determine the severity of hemorrhage in patients with Bernard-Soulier syndrome.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    HADJATI, S., FARSINEJAD, A., FARANOUSH, M., GHAREHBAGHIAN, A., AMIRIZADEH, N., & TOOGEH, GH.. (2014). QUANTITATIVE IMMUNOPHEMOTYPING OF PLATELET SURFACE GLYCOPROTEINS AMONG IRANIAN PATIENTS WITH BERNARD-SOULIER SYNDROME. IRANIAN JOURNAL OF BLOOD AND CANCER (IJBC), 7(1), 3-9. SID. https://sid.ir/paper/313231/en

    Vancouver: Copy

    HADJATI S., FARSINEJAD A., FARANOUSH M., GHAREHBAGHIAN A., AMIRIZADEH N., TOOGEH GH.. QUANTITATIVE IMMUNOPHEMOTYPING OF PLATELET SURFACE GLYCOPROTEINS AMONG IRANIAN PATIENTS WITH BERNARD-SOULIER SYNDROME. IRANIAN JOURNAL OF BLOOD AND CANCER (IJBC)[Internet]. 2014;7(1):3-9. Available from: https://sid.ir/paper/313231/en

    IEEE: Copy

    S. HADJATI, A. FARSINEJAD, M. FARANOUSH, A. GHAREHBAGHIAN, N. AMIRIZADEH, and GH. TOOGEH, “QUANTITATIVE IMMUNOPHEMOTYPING OF PLATELET SURFACE GLYCOPROTEINS AMONG IRANIAN PATIENTS WITH BERNARD-SOULIER SYNDROME,” IRANIAN JOURNAL OF BLOOD AND CANCER (IJBC), vol. 7, no. 1, pp. 3–9, 2014, [Online]. Available: https://sid.ir/paper/313231/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