Borderline HbA2 levels: dilemma in diagnosis of beta-thalassemia carriers
There is inconsistency in the exact definition of diagnostic levels of HbA 2 for β thalassemia
trait. While many laboratories consider HbA 2≥ 4.0% diagnostic, still others consider HbA …
trait. While many laboratories consider HbA 2≥ 4.0% diagnostic, still others consider HbA …
[HTML][HTML] Differentiation of beta thalassemia trait from iron deficiency anemia by hematological indices
Objective: We aimed at finding out reliable parameter in the differentiation of iron deficiency
anemia (IDA) and beta-thalassemia trait (β-TT) in the adult population subjected to Saudi …
anemia (IDA) and beta-thalassemia trait (β-TT) in the adult population subjected to Saudi …
Discrimination of β-thalassemia and iron deficiency anemia through extreme learning machine and regularized extreme learning machine based decision support …
Abstract The symptoms of Iron Deficiency Anemia (IDA) and β-thalassemia (β-TT) disease
are similar and the distinction between them is time consuming and costly. There are several …
are similar and the distinction between them is time consuming and costly. There are several …
Unresolved laboratory issues of the heterozygous state of β-thalassemia: A literature review
S Thilakarathne, UP Jayaweera… - …, 2023 - pmc.ncbi.nlm.nih.gov
Although considered a mild clinical condition, many laboratory issues of the carrier state of β-
thalassemia remain unresolved. Accurate laboratory screening of β-thalassemia traits is …
thalassemia remain unresolved. Accurate laboratory screening of β-thalassemia traits is …
[HTML][HTML] Undiagnosed hemoglobinopathies: a potential threat to the premarital screening program
Objectives: To evaluate the prevalence of undiagnosed hemoglobinopathies among
individuals visiting the premarital screening Centre. Methods: This study was conducted at …
individuals visiting the premarital screening Centre. Methods: This study was conducted at …
ThalPred: a web-based prediction tool for discriminating thalassemia trait and iron deficiency anemia
V Laengsri, W Shoombuatong, W Adirojananon… - BMC medical informatics …, 2019 - Springer
Background The hypochromic microcytic anemia (HMA) commonly found in Thailand are
iron deficiency anemia (IDA) and thalassemia trait (TT). Accurate discrimination between …
iron deficiency anemia (IDA) and thalassemia trait (TT). Accurate discrimination between …
Hemoglobin A2 (HbA2) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT)
AM Al-Amodi, NZ Ghanem, SA Aldakeel… - … medical research and …, 2018 - Taylor & Francis
Introduction: Detection of β-thalassemia trait or carriers (β-TT) depends significantly on an
increase in Hemoglobin A2 (HbA2) levels, which is found at low levels (< 3%) in normal …
increase in Hemoglobin A2 (HbA2) levels, which is found at low levels (< 3%) in normal …
[HTML][HTML] Spectrum of hemoglobinopathies with hematological and biochemical profile: A five year experience from a tertiary care hospital
N Mansoor, F Meraj, A Shaikh… - Pakistan Journal of …, 2022 - ncbi.nlm.nih.gov
Methods: This retrospective study included results of high performance liquid
chromatography (HPLC) test from July 2015-May 2020 in the department of Hematology …
chromatography (HPLC) test from July 2015-May 2020 in the department of Hematology …
Screening of extended family members of thalassemia major children as a thalassemia preventive strategy
ND Sonkawade, AA Kinikar, RK Kulkarni… - Ethiopian Journal of …, 2022 - ajol.info
BACKGROUND: Thalassemia is considered as the most common single gene disorder
worldwide. Preventive measures include identification of thalassemia carriers (traits) through …
worldwide. Preventive measures include identification of thalassemia carriers (traits) through …
Candidate SNP Markers of Chronopathologies Are Predicted by a Significant Change in the Affinity of TATA‐Binding Protein for Human Gene Promoters
Variations in human genome (eg, single nucleotide polymorphisms, SNPs) may be
associated with hereditary diseases, their complications, comorbidities, and drug responses …
associated with hereditary diseases, their complications, comorbidities, and drug responses …