Overview on thalassemias: a review article

DC Sharma, A Arya, P Kishor, P Woike… - Medico Research …, 2017 - medrech.com
Thalassemia's are genetic disorders inherited from a person's parents. Thalassemia's are
prevalent worldwide with 25,000 deaths in 2013. Highest rates are in the Mediterranean …

[HTML][HTML] Reliability of different RBC indices and formulas in discriminating between β-thalassemia minor and other microcytic hypochromic cases

E Bordbar, M Taghipour, BE Zucconi - Mediterranean journal of …, 2015 - ncbi.nlm.nih.gov
Objective Different indices and formulas of CBC parameters have been suggested as
indicators of early stage screenings to detect couples with β-thalassemia minor (BTMi). In …

An overview on thalassemia: A review article

MA Meri, AH Al-Hakeem… - Medical …, 2022 - medical.science.journal-asia …
Thalassemia is a hereditary blood disorder which is passed down through families in which
the body makes an abnormal form of hemoglobin. This disorder results in the destruction of …

[HTML][HTML] Frequency of thalassemia in Iran and Khorasan Razavi

GH Khodaei, N Farbod, B Zarif, S Nateghi… - International journal of …, 2013 - ijp.mums.ac.ir
Introduction: Beta-thalassemia is the most common hereditary disease in Iran. More than two
million carriers of beta-thalassemia live in Iran. Since the Iranian population is a mixture of …

Hemoglobinopathy carrier prevalence in the United Arab Emirates: first analysis of the Dubai Health Authority premarital screening program results

KM Belhoul, M Abdulrahman, RF Alraei - Hemoglobin, 2013 - Taylor & Francis
The aim of this study was to determine the prevalence of hemoglobinopathy carriers in
United Arab Emirates (UAE) nationals subjected to mandatory premarital screening in Dubai …

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 …

Two decades of pre-marital screening for beta-thalassemia in central Iran

M Zeinalian, RF Nobari, A Moafi, M Salehi… - Journal of community …, 2013 - Springer
Thalassemia is the most widespread recessive disease worldwide (Ryan et al. 2010;
Weatherall and Clegg 2001). Beta-thalassemia is characterized by the deficiency or …

The effect of mother's β-thalassemia minor on placental histology and neonatal outcomes

H Vafaei, S Karimi, M Akbarzadeh Jahromi… - The Journal of …, 2022 - Taylor & Francis
Objective β-thalassemia is a prevalent disease in Iran. The adverse effects of anemia on
placental and neonatal outcomes have previously been shown. Women require additional …

Thalassemia gene mutations in Kohgiluyeh and Boyer-Ahmad province

J Pouranfard, F Vafaei, S Afrouz, M Rezaeian - Iranian Journal of Blood and …, 2020 - ijbc.ir
Background: Thalassemia is the most common hereditary anemia which has a relatively
high prevalence in Iran. In most cases, more than 300 mutations have been identified, which …

Knowledge and Attitude toward Hemoglobinopathies in Premarital Screening Program among the General Population in the Western Region of Saudi Arabia

HA Almasmoum, A Tabassum, MS Iqbal… - …, 2022 - Taylor & Francis
Abstract The National Premarital Screening Program, which includes sickle cell disease and
thalassemia, was made mandatory in 2004 by the Kingdom of Saudi Arabia (KSA), and the …