Global distribution of β-thalassemia mutations: An update

E Rao, SK Chandraker, MM Singh, R Kumar - Gene, 2024 - Elsevier
One excellent illustration of how a single gene abnormality may result in a spectrum of
disease incidence is the incredible phenotypic variety of β-thalassemia, which spans from …

Molecular epidemiology and hematologic characterization of thalassemia in Guangdong Province, Southern China

J Xian, Y Wang, J He, S Li, W He… - Clinical and Applied …, 2022 - journals.sagepub.com
Introduction: About 2% of the population in the world are carriers of the thalassemia gene.
Thalassemia is highly prevalent in Southern China, and traditional clinical testing methods …

[HTML][HTML] Hemoglobinopathies in Iran: an updated review

A Nasiri, Z Rahimi, A Vaisi-Raygani - International Journal of …, 2020 - ncbi.nlm.nih.gov
Hemoglobinopathies are the most common single gene disorders (monogenic disorders) in
the world population. Due to specific position of Iran and the presence of multi-ethnic groups …

Beta thalassemia in 31,734 cases with HBB gene mutations: pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East

N Mahdieh, B Rabbani - Blood reviews, 2016 - Elsevier
Thalassemia is one of the most common single gene disorders worldwide. Nearly 80 to 90
million with minor beta thalassemia and 60–70 thousand affected infants are born annually …

[HTML][HTML] Cut off determination of discrimination indices in differential diagnosis between iron deficiency anemia and β-thalassemia minor

E Miri-Moghaddam, N Sargolzaie - International journal of …, 2014 - ncbi.nlm.nih.gov
Objective The two most frequent hypochromic microcytic anemias are β-thalassemia minor
(BTM) and iron deficiency anemia (IDA). Several discrimination indices have been proposed …

[HTML][HTML] Causes of new cases of major thalassemia in sistan and balouchistan province in South-East of iran

E Miri-Moghaddam, M Naderi, S Izadi… - Iranian journal of …, 2012 - ncbi.nlm.nih.gov
Background Thalassemia is the most common monogenic disease in South-East of Iran.
Despite the 70% reduction in Iranian thalassemia cases after thalassemia control …

Genetic epidemiology, hematological and clinical features of hemoglobinopathies in Iran

Z Rahimi - BioMed research international, 2013 - Wiley Online Library
There is large variation in the molecular genetics and clinical features of
hemoglobinopathies in Iran. Studying structural variants of hemoglobin demonstrated that …

[HTML][HTML] High school knowledge and attitudes towards thalassemia in southeastern Iran

E Miri-Moghaddam, E Motaharitabar… - … -Oncology and Stem …, 2014 - ncbi.nlm.nih.gov
Objectives Thalassemia (thal) is the most single gene disorders in southeast of Iran. About
one quarter of total Iranian new thal cases were born in the Sistan and Balouchistan …

Health-related quality of life and associated factors among thalassemia major patients, Southeast of Iran

A Bazi, O Sargazi-Aval, A Safa… - Journal of Pediatric …, 2017 - journals.lww.com
Low quality of life (QOL) is a feature that has been overlooked in thalassemia major (TM)
patients. Our aim was to assess QOL in school-aged TM patients in Zabol city and …

[HTML][HTML] Survival analysis and its associated factors of Beta thalassemia major in hamadan province

R Zamani, S Khazaei, S Rezaeian - Iranian journal of medical …, 2015 - ncbi.nlm.nih.gov
Background There currently is a lack of knowledge about the long-term survival of patients
with beta thalassemia (BT), particularly in regions with low incidence of the disease. The aim …