Evalution of HbA۲ In Minor β Thalassemia Carriers Reffered to Kerman Special Disease Center
سال انتشار: 1382
نوع سند: مقاله ژورنالی
زبان: فارسی
مشاهده: 114
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شناسه ملی سند علمی:
JR_JKMU-10-4_006
تاریخ نمایه سازی: 16 اسفند 1402
چکیده مقاله:
Increased HbA۲ is a characteristic finding in minor beta thalassemia. Minor β-thalassemia is a heterozygote form of β-thalassemia that carries thalassemia genes but does not cause thalassemia disease. Diagnosis of carriers is done by CBC, RBC Index, and HbA۲ test. Very few cases of people with minorthalassemia have a normal HbA۲. 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 HbA۲ . All of the people with normal HbA۲ 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.
کلیدواژه ها:
نویسندگان
M Atapour
Medical Laboratory Doctor, Kerman University of Medical Sciences and Health Services, Kerman, Iran
AR Zohoor
Assistant Professor of Epidemiology, Iran University of Medical Sciences and Health Services, Tehran, Iran
A Zolala
B.Sc. in Medical Laboratory Science
AR Arjmand
M.Sc. Student of Hemathology, Tarbiat Moddares University, Tehran, Iran