β-THALASSEMIA TRAIT MENGGUNAKAN ELEKTROFORESIS MIKROKAPILER
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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xxx (14.5%). These differences may be explained by the different types of equipment on the market today where the cell measurement methods may be different. Regarding erythrogram and leukogram parameters, the values found for both women and men did not show significant differences compared to values reported in the literature.(1,2,8) Reference values, stratified by gender, are described in Tabl...
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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 ...
متن کاملPrevalence of β thalassemia carrier state in Sindhi community of Wardha and evaluation of risk factors for β thalassemia trait.
OBJECTIVE To determine the prevalence of β thalassemia in Sindhi community of Wardha and evaluation of risk factors. To give genetic counseling to those diagnosed as carriers. STUDY DESIGN Cross-sectional (prevalence study). SETTING Sindhi community residing in and around Wardha. STUDY PERIOD 18 months. MATERIALS AND METHODS A total of 578 individuals belonging to Sindhi community resid...
متن کاملDid the Proband Have Thalassemia Intermedia or Severe Thalassemia Trait?
I enjoyed reading Bilgen et al.’s case report, The effect of HBB: (c*+96T>C (3’UTR+1570 T>C) on the mild β-thalassemia intermedia pheonotype, in the recent issue of the Journal (2011; 28: 219-222). I congratulate the authors for exploring at the molecular level at least one of the thalassemia minima that fits well with the present clinical thalassemia nomenclature. Based on their clinical descr...
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ژورنال
عنوان ژورنال: INDONESIAN JOURNAL OF CLINICAL PATHOLOGY AND MEDICAL LABORATORY
سال: 2018
ISSN: 2477-4685,0854-4263
DOI: 10.24293/ijcpml.v21i2.1103