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Information Journal Paper

Title

EVOLUTION OF HBA2 IN MINOR B THALASSEMIA CARRIERS REFFERED TO KERMAN SPECIAL DISEASE CENTER

Pages

  99-104

Keywords

HBA2Q4

Abstract

 Increased HbA2 is a characteristic finding in minor beta thalassemia. Minor b-thalassemia is a heterozygote form of b-thalassemiathat carries thalassemia genes but does not cause thalassemia disease. Diagnosis of carriers is done by CBC, RBC Index, and HbA2 test. Very few cases of people with minor-thalassemia have a normal HbA2. According to the results of this pilot study it seams that percentage of MINOR THALASSEMIA is noticeable in Kerman province. In this survey parents of thalassemia major and intermedia were evaluated. The result showed that about two percent of them had normal HbA2. All of the people with normal HbA2 were born. in Kerman. We suggest that this type of study should be done in different cities of this province in order to take necessary steps in effective prevention of major-thalassemia.

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    APA: Copy

    ATAPOUR, M., ZOHOUR, A.R., ZOU ALALI, A., & ARJMAND, A.R.. (2003). EVOLUTION OF HBA2 IN MINOR B THALASSEMIA CARRIERS REFFERED TO KERMAN SPECIAL DISEASE CENTER. JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES, 10(2), 99-104. SID. https://sid.ir/paper/503/en

    Vancouver: Copy

    ATAPOUR M., ZOHOUR A.R., ZOU ALALI A., ARJMAND A.R.. EVOLUTION OF HBA2 IN MINOR B THALASSEMIA CARRIERS REFFERED TO KERMAN SPECIAL DISEASE CENTER. JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2003;10(2):99-104. Available from: https://sid.ir/paper/503/en

    IEEE: Copy

    M. ATAPOUR, A.R. ZOHOUR, A. ZOU ALALI, and A.R. ARJMAND, “EVOLUTION OF HBA2 IN MINOR B THALASSEMIA CARRIERS REFFERED TO KERMAN SPECIAL DISEASE CENTER,” JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES, vol. 10, no. 2, pp. 99–104, 2003, [Online]. Available: https://sid.ir/paper/503/en

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