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Relevant bibliographies by topics / BETA-THALASSEMIA TRAIT

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Academic literature on the topic 'BETA-THALASSEMIA TRAIT'

Author: Grafiati

Published: 11 March 2023

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Journal articles on the topic "BETA-THALASSEMIA TRAIT"

1

Khan, Muhammad Ihtesham, Hamid Nawaz Khan, and Muhammad Usman. "BETA THALASSEMIA TRAIT;." Professional Medical Journal 25, no. 04 (2018): 545–50. http://dx.doi.org/10.29309/tpmj/18.4347.

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2

Khan, Muhammad Ihtesham, Hamid Nawaz Khan, and Muhammad Usman. "BETA THALASSEMIA TRAIT." Professional Medical Journal 25, no. 04 (2018): 545–50. http://dx.doi.org/10.29309/tpmj/2018.25.04.343.

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Objectives: To assess the sensitivity of the various discrimination indicesas screening test in beta-thalassemia trait patients in our population. Study design: Crosssectional descriptive study. Period: 1-Sep 2012 to 31-Jan 2013 (5 months). Settings: PathologyDepartment, District Head Quarters (DHQ) Hospital, Rawalpindi. Materials and Methods: Atotal of 150 diagnosed cases of beta thalassemia trait were included in the study. Study wasdone from 1-Sep 2012 to 31-Jan 2013 in DHQ hospital, Rawalpindi. Four discrimination indicesi.e. Mentzer, Shine & Lal, Srivastava, and Red cell Distribution

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3

Setiadji, Vinisia, Bidasari Lubis, Adi Koesoema Aman, and Herman Hariman. "DISCREPANCY BETWEEN HAEMOGLOBIN, RDW, AND MEAN CORPUSCULAR VALUES IN PATIENTS WITH BETA THALASSEMIA / HEMOGLOBIN E DISEASE AND BETA THALASSEMIA TRAIT." INDONESIAN JOURNAL OF CLINICAL PATHOLOGY AND MEDICAL LABORATORY 25, no. 3 (2019): 343. http://dx.doi.org/10.24293/ijcpml.v25i3.1459.

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Thalassemia beta / hemoglobin E adalah suatu kondisi dengan heterozigot ganda gen pembawa thalassemia beta dan hemoglobin E. Hal ini menyebabkan kondisi dengan gambaran fenotip yang berat dibandingkan trait thalassemia beta dan trait hemoglobin E. Secara logika, nilai mean corpuscular dari thalassemia beta / hemoglobin E seharusnya memburuk. Pada penelitian ini, kami meneliti sebelas kasus dari dua keluarga dengan anggota menderita thalassemia beta / hemoglobin E.Pada keluarga-1 dua anggota dengan trait thalassemia beta memiliki nilai MCV 68 fL dan 65 fL, dan nilai MCH 21 pg dan 20 pg. Pada ke

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4

Rahman, MMU, M. Nayem, W. Begum, FA Begum, MNU Ahmed, and S. Sultana. "Pattern of Red Cell Count and Red Cell Distribution Width (RDW %) in Beta Thalassaemia Trait in Adults." Bangladesh Journal of Medical Biochemistry 9, no. 1 (2018): 31–35. http://dx.doi.org/10.3329/bjmb.v9i1.36152.

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Microcytic hypochromic anemia is one of the commonest hematological abnormalities in Bangladeshi population. Iron deficiency anemia and beta thalassemia traits are the most frequent causes of microcytic hypochromic anemia which are sometimes difficult to differentiate clinically and by routine laboratory examinations due to similar blood picture. To differentiate between patients of beta thalassemia trait and iron deficiency anemia, physicians need a group of investigations including peripheral blood film, estimation of HbA2, serum ferritin, serum iron, total iron binding capacity and transfer

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5

Shalli, Awaz Ahmed Kamal, Sana Dlawar Jalal, and Dler Jaza Mohammed. "The impact of iron deficiency on the diagnostic level of HbA2 in beta- thalassemia trait from the Sulaimani hemoglobinopathies screening program." Advanced medical journal 7, no. 1 (2022): 95–100. http://dx.doi.org/10.56056/amj.2022.164.

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Background and objectives: The identification of carriers of beta- thalassemia depends on the detection of a high level of hemoglobin A2. The hemoglobin A2 level is influenced by some elements including iron. The consequence of concomitant iron deficiency on the hemoglobin A2 level is critical in screening laboratories for hemoglobinopathies, particularly in resource-limited ones where molecular identification of hemoglobin A2 levels is unavailable. The aim of this study is to evaluate the consequence of iron deficiency on hemoglobin A2 level to obtain a definite diagnosis of beta- thalassemia

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6

Bhatt, Rajendra Dev. "Report of Beta Thalassemia in Newar Ethinicity." Annals of Clinical Chemistry and Laboratory Medicine 3, no. 1 (2018): 30–34. http://dx.doi.org/10.3126/acclm.v3i1.17298.

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Beta thalassemia trait is a heterogeneous autosomal recessive form of beta thalassemia. Individual with beta thalassemia are clinically asymptomatic. Here we have described a case that has been incidentally diagnosed as beta thalassemia trait. A 31 year old male form Newar Community came to hospital for routine health checkup was send for hematological investigation. On examination, his red cell morphology was found to be microcytic hypochromic and his hemoglobin concentration was mildly decrease. His other parameters was evaluated and requested for analysis of iron profile and hemoglobin elec

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7

Dutta, Shyamali, Tuphan Dolai, Rajat Kumar, et al. "Are Red Cell Indices a Reliable Screening Tool in Pre-Natal Screening for the Avoidance of E-Beta Thalassemia and Beta Thalassemia Major Births? Results of a Population Survey From Eastern India." Blood 118, no. 21 (2011): 5303. http://dx.doi.org/10.1182/blood.v118.21.5303.5303.

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Abstract Abstract 5303 The state of West Bengal in the eastern part of India has a high prevalence of the carrier states of beta thalassemia and Hb E. Analysis of Hb HPLC screening data from 200 individuals, including adults and children from urban areas around Kolkata in West Bengal, carried out in our institution1, reveals a prevalence 6.5% for beta trait and 5.5% for HbE trait. (unpublished data) It may be possible to reduce births of beta thalassemia major and E beta thalassemia by preventive strategies, including mass screening and awareness campaigns. The best preventive method is debata

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8

Kotila, Taiwo R. "Sickle Cell Trait: A Benign State?" Acta Haematologica 136, no. 3 (2016): 147–51. http://dx.doi.org/10.1159/000446526.

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Background: Sickle cell trait (SCT) is the heterozygous form of sickle cell disease and expectedly should be a benign state with no complications ascribed to it. There are numerous reports challenging its being a benign condition, though this is controversial. Methods and Results: A review of the results of the accompanying investigations done on some of the patients show that beta thalassemia may be responsible for many of the ascribed symptoms and complications. These patients may therefore have sickle cell beta thalassemia, a compound heterozygous form of sickle cell disease. Conclusion: It

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9

Akasheh, M. S. "Graves' disease mimicking beta-thalassemia trait." Postgraduate Medical Journal 70, no. 822 (1994): 300–301. http://dx.doi.org/10.1136/pgmj.70.822.300.

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10

Shahid, Hassnain, Maryam Saleem, Nauman Naseer, Samina Tabussam, Atif Aziz, and Saeed Ullah. "Evaluation of Srivastava index to distinguishing Beta-Thalassemia Trait from Iron Deficiency." Pakistan Journal of Medical and Health Sciences 16, no. 5 (2022): 1225–27. http://dx.doi.org/10.53350/pjmhs221651225.

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Objective: To assist in the differential diagnosis of beta thalassemia trait and iron deficiency anaemia, many alternative red blood cell index-based formulae were examined. Methods: The Rawalpindi PEMH performed this study from June 2021 to March 2022. For individuals with beta- thalassemia trait and iron deficient anaemia, age and gender were not considered. More than five millilitres of blood were drawn from each patient in order to determine the haemoglobin content, the number of red blood cells, how they were distributed, and the average cell volume. Five alternative formulas may be used

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