Reticulocyte evaluation in α+-thalassemia
نویسندگان
چکیده
منابع مشابه
Using Reticulocyte Indices to Identify Α-thalassemia– a Preliminary Report
Thalassemia poses an important public health problem in Thailand. The Ministry of Public Health of Thailand has conducted many programs for the control of thalassemia. These programs are useless if there is no effective, affordable method of screening for carriers. We report on the possibility of using an automated reticulocyte analyzer in order to identify α-thalassemia. Thirty-one control sub...
متن کاملMolecular Basis of α-Thalassemia in Iran
Alpha-thalassemia (α-thal) is probably the most prevalent monogenic condition in the world. Deletions are the most common types of mutations in α-thal, followed by point mutations and small insertion/deletion. In the context of national screening program for prevention of thalassemia and hemoglobinopathies in Iran, α-thal carriers have come to more attention. Therefore, the fr...
متن کاملReticulocyte hemoglobin equivalent to detect thalassemia and thalassemic hemoglobin variants
INTRODUCTION Thalassemia and iron deficiency may both result in hypochromic microcytic anemia. Hematological algorithms that differentiate the two are mainly established in adult selected diagnostic groups. We aimed at creating an algorithm applicable in the presence of children, hemoglobin variants, and iron deficiency. METHODS Our study material constituted blood samples referred during 1 y...
متن کاملClinical manifestations of α-thalassemia.
α-Thalassemia mutations affect up to 5% of the world's population. The clinical spectrum ranges from an asymptomatic condition to a fatal in utero disease. Hemoglobin H disease results from mutations of three α-globin genes. Deletional forms result in a relatively mild anemia, whereas nondeletional mutations result in a moderate to severe disease characterized by ineffective erythropoiesis, rec...
متن کاملMolecular Basis of α-Thalassemia in Iran
Alpha-thalassemia (α-thal) is probably the most prevalent monogenic condition in the world. Deletions are the most common types of mutations in α-thal, followed by point mutations and small insertion/deletion. In the context of national screening program for prevention of thalassemia and hemoglobinopathies in Iran, α-thal carriers have come to more attention. Therefore, the frequency and distri...
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ژورنال
عنوان ژورنال: American Journal of Hematology
سال: 2005
ISSN: 0361-8609,1096-8652
DOI: 10.1002/ajh.20487