Define Alpha-thalassemia. Alpha-thalassemia synonyms, Alpha-thalassemia pronunciation, Alpha-thalassemia translation, English dictionary definition of Alpha-thalassemia. n. An inherited form of anemia occurring chiefly among people of Mediterranean desce
(MD) and confidence intervals 95% (CI 95%) were calculated by the random effect model for beta-thalassemia major (BTM) (1351 subjects: 770 thalassemic and 581 controls, from 15 studies) and Trait (BTT) or Hemoglobin E (BTE) (475 subjects: 165 thalassemic and 310 controls, from 5 ...
Int J Lab Hematol 2016;38(suppl 1):20–26. 33. Galanello R, Melis MA, Ruggeri R, et al. Beta 0 thalassemia trait in Sardinia. Hemoglobin 1979;3:33–46. 34. Danjou F, Anni F, Galanello R. Beta-thalassemia: from genotype to phenotype. Haematologica 2011;96:1573–1575...
Of interest is the results of multiple logistic regression analysis which indicated that either one α-gene defect, two α-gene defects, Hb E trait, or homozygous Hb E were important risk factors of anemia in this studied population. The findings of greater association with anemia of two α-...
α-thal-2, and α-thal-1, i.e., she had HbS trait together with HbH disease or aoαo/αoα; β/βs The results were compared with those of similar experiments on the DNA of a Laotian child with HbE trait, Hb Constant Spring, and α-thalassemia-1 trait or ααcs/αoαo;β/...
Chinese Gγ+(Aγδβ)0-thalassemia and SEA-HPFH are the most common types of β-globin gene cluster deletion in Chinese population. The aim of the study was to analyze clinical features of deletional Chinese Gγ+(Aγδβ)0-thalassemia and Southeast Asian hereditary persistence of fetal hemo...
. 18 Hematological values & a-Thalassemia Hematological values & a-Thalassemia Molecular diagnosis of hemoglobin disorders, Clin. Lab. Haem. 2004, 26, 159–176 a a a a s 19 Thalassemia Major Thalassemia Major 20 an inherited form of hemolytic anemia an inherited form of hemolytic anemia red ...
IntroductionThe potential impact of concomitant iron deficiency on hemoglobin A2 (HbA2)-based identification of β-thalassemia trait (βTT) is a worrisome issue for screening laboratories. This is especially true for resource-constrained settings where iron deficiency is widespread and molecular ...
Alpha-haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of beta-thalassaemia. Br J Haematol 2006;133:675– 682. 68. Galanello R, Perseu L, Giagu N, Sole G, Perra C. AHSP expression in beta thalassemia carriers with thalassemia intermedia phenotype. Blood...
Class selection has been used due to characteristics of the silent trait having identical CBC values compared to non-carriers. It was done to see if statistical tests indicate a difference between the two classes or if grouping them would be beneficial. For this, the Mann–Whitney U test has...