Double heterozygosity for hemoglobin MalmoĢ [beta 97 (FG 4) His-->Gln] and beta-thalassemia traits
, 1989 A 32-year-old Sicilian man had marked erythrocytosis (Hb = 23.0 g/dl, RBC = 10.5 x 10(12)/l, MCV = 71 fl, Hct = 84-92%, a 4.5 times increase in total erythropoies) and saphenous system varices, without other clinical abnormalities. By Hb electrophoresis,
A. Riccardi +4 more
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The Efficacy of Mitapivat in Case of Transfusion Dependence Linked to Beta Thalassemia Trait Associated with Pyruvate Kinase Deficiency. [PDF]
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Autosomal Recessive Hyper-IgE Syndrome in a Child With Beta Thalassemia Trait: A Case Report. [PDF]
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Exploring the Clinical and Hematological Characteristics of Beta-Thalassemia Trait: A Comprehensive Analysis in a Tertiary Care Hospital Setting. [PDF]
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A New Formula Based on Simple Blood Indices to Differentiate Beta Thalassemia Trait from Iron Deficiency Anemia. [PDF]
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Distinguishing Iron Deficiency Anemia From Beta-Thalassemia Trait: Comparative Analysis of CRUISE Index and Other Traditional Diagnostic Indices. [PDF]
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Differentiation of beta thalassemia trait from iron deficiency anemia by hematological indices. [PDF]
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Prevalence and assessment of the impact of iron-deficiency anemia in beta-thalassemia trait subjects: A study from a tertiary care center of Western India. [PDF]
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The role of discriminant functions in screening beta thalassemia trait and iron deficiency anemia among laboratory samples. [PDF]
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