Diamond–Blackfan anemia associated with β-thalassemia trait
نویسندگان
چکیده
منابع مشابه
Low HbA2 Level in β-Thalassemia Trait
Dr. Köseler and her colleagues reported the presence of δthalassemia in 3 out of 12 patients carrying the β-thalassemia trait with low HbA2 in the recent issue of this journal without giving any explanations for the remaining 9 cases (2012; 29: 289-290) [1]. I wish that they would also look for the presence of αthalassemia, at least in those 9 cases, because this seems to be the more prevalent ...
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Hemoglobin E (HbE) β-thalassemia is the most common severe thalassemia syndrome across Asia, and millions of people are carriers. Clinical heterogeneity in HbE β-thalassemia is incompletely explained by genotype, and the interaction of phenotypic variation with hepcidin is unknown. The effect of thalassemia carriage on hepcidin is also unknown, but it could be relevant for iron supplementation ...
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I N 1955 RIGAS ET AL.1 and Gouttas et al.2 independently reported the discovery of a new hemoglobin characterized electrophoretically at pH 8.6 by a more rapid anodal mobility than that of normal adult hemoglobin. This hemoglobin has subsequently been identified by the letter “H.” More recently, “fast” hemoglobins other than “H” have been described. These include hemoglobins J,3 J,4-1#{176} K,5...
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Sickle cell-thalassemia associated with glucose- 6-phosphate dehydrogenese deficiency is reported in an Iranian family. The father had sickle trait and G.6.P.D. deficiency, the mother minor thalassemia, one of the sons siclc:le ceH-thailasemiia., the oth-er sickle cell trait; the daughter had sickle cell-thalassemia and was carrier of G.6.P.D. deficiellcy.
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ژورنال
عنوان ژورنال: American Journal of Hematology
سال: 2006
ISSN: 0361-8609,1096-8652
DOI: 10.1002/ajh.20530