thalassemia minor
Cut off Determination of Discrimination Indices in Differential Diagnosis between Iron Deficiency Anemia and β- Thalassemia Minor.
... β Thalassemia Minor (BTM) and Iron deficiency anemia (IDA) are the most commonly encountered with mild hypochoromic microcytic ...β thalassemia (β thal) major baby birth and minimization of ...β ...
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Value of Cell Counter-Based Parameters and Formulas in Detection of β-Thalassemia Minor, the experience of a single Haematological Centre in Iraq
... beta thalassemia minor and other types of hypochromic microcytic ...beta thalassemia minor and other types of hypochromic microcytic ...between thalassemia trait and other hypochromic ...
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Determination of Lipid Profile in Preschool Children and Pre-College Students with Beta-Thalassemia Minor and Control Group
... of minor thalassemia as cut-off Point HbA 2 ≥ ≥ ≥ ≥ ≥ ...of minor thalassemic patients, serum lipids (TG, cholesterol, HDL, LDL) for them and control group were ...between minor thalassemic ...
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Premarital Screening of Beta Thalassemia Minor in north-east of Iran
... beta-thalassemia minor in the other areas of the Iran to perform genetic counseling and perinatal diagnosis seems ...essential. Thalassemia is found in some 60 countries with the highest prevalence ...
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Beta Thalassemia Minor as a Risk Factor for Suicide and Violence: A Failure to Replicate
... in thalassemia minor, at a population ...where thalassemia trait is ...β-thalassemia minor pheno- type with suicide, aggression and ...
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Potassium permeability in β thalassemia minor red blood cells
... the thalassemia minor cells but does not follow comparable depletion in normal ...incubated thalassemia minor red blood cells to osmotic ...
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HBB FSC 36-37 (-T) Gene Mutation Detection in Carriers of Thalassemia Minor Using High Resolution Melting Analysis
... Commonly used techniques for molecular diagnosis of β-thalassemia subjects include PCR-based strategies consisting of high performance liquid chromatography (HPLC) (Reichert et al., 2008), capillary ...
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The Prevalence of Thalassemia Minor in The Aliabad Katool
... Thalassaemia in the Greek community of Cape Town. Prevalence of thalassaemia in schoolchildren in north-eastern Badia , Jordan. Premarital screening of beta – thalassemia trait in[r] ...
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ELECTROPHORETIC COMPONENTS OF THE HEMOGLOBIN OF RED CELL MEMBRANES
... Electrophoretic analyses of the membrane hemoglobin of four individuals with thalassemia minor disclosed an increased amount of hemoglobin A2 in the membrane pigment; however, the relati[r] ...
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The pregnancy outcome in patients with minor β-thalassemia
... This was a case-control study which included all the pregnancies (7290) referring to Hafez and Zeinabieh Hospitals of Shiraz University of Medical Sciences between 2006 and 2008. The patients were divided into two groups ...
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Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia
... Hemoglobin A2 (Hb A2), is a minor adult hemoglobin, its levels ranged between (2–3.2%) of the total circulating haemoglobin in healthy adults [10]. The increase in Hb A2 level more than borderline levels is the ...
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Beta-thalassemia
... of thalassemia minor subjects is ...with thalassemia intermedia who do not usually have severe hemosiderosis are less prone to cardiac prob- lems ...
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FURTHER STUDIES ON THE GENETICS OF THALASSEMIA
... patients with Italian antecedents in Rochester, and found six (0.06) com- patible with thalassemia minor. Four of these smears were followed u p with complete blood an[r] ...
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Relationship of Thyroid Hormone Status with Iron Overload in the Βeta-Thalassemic Tribal Children Receiving Multiple Blood Transfusions- A Cross-Sectional Descriptive Study
... Thalassemia, a major public health problem in India, especially in tribal populations, is an autosomal recessive inherited blood disorder in which blood transfusion is the mainstay of treatment which in turn may ...
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Beliefs about chelation among thalassemia patients
... of thalassemia are not only associated with higher sensi- tive Soma scores but also impaired quality of life ...that thalassemia patients on both types of chelators express an understanding of the need for ...
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Haematological and Genetic Characterization of Thalassemia Intermedia in Tank and South Waziristan Agency of Khyber Pakhtun Khwa
... β thalassemia intermedia do not require blood transfusion except when they develop infections, which augment .... Thalassemia intermedia is a rare condition and very little work has been done in ...β ...
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Mild thalassemia: the result of interactions of alpha and beta thalassemia genes
... Homozygous thalassemia is due to inherited unbalanced synthesis of the a- or b-chains of ...concept. Thalassemia in these individuals was evaluated by clinical and genetic ...
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... Female patients with sickle cell-β-thalassemia may have reduced fertility, but pregnancy occurs and is associated with high degree of maternal morbidity and fetal wastage [21]. In the present study, some β- ...
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Phosphaturia in Thalassemia
... in four thalassemic children aged 6 to 10 years. No correla- tioi was found between phosphorus intake and serum level or betwceii 1)liosPliortts intake and net absorption. There was a po[r] ...
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Thalassemia: A Review
... The thalassemias are a diverse group of genetic blood diseases characterized by absent or decreased production of normal hemoglobin, resulting in a microcytic anemia of varying degree. The thalassemias have a ...
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