Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population

FA Noor, N Sultana, GS Bhuyan, MT Islam… - Orphanet journal of rare …, 2020 - Springer
Background ß-thalassemia is one of the most common inherited blood disorders in the world
and a major deterrent to the public health of Bangladesh. The management of thalassemia …

[HTML][HTML] Hypothyroidism and hypoparathyroidism in thalassemia major patients: a study in Sistan and Baluchestan Province, Iran

A Bazi, H Harati, A Khosravi-Bonjar… - … of Endocrinology and …, 2018 - ncbi.nlm.nih.gov
Objectives In the present study, we assessed the frequency of HT and HPT in a population of
TM patients in Southeast of Iran. Methods This cross sectional study was performed on 194 …

The‑α3. 7 deletion in α‑globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population

JF Borgio, S Abdulazeez… - Molecular …, 2018 - spandidos-publications.com
Abstract The regions of Al‑Qatif and Al‑Ahssa in the Eastern Province of Saudi Arabia are
known for their high prevalence of hemoglobinopathies, including β‑thalassemia and sickle …

[HTML][HTML] Cholelithiasis in thalassemia major patients: a report from the South-East of Iran

I Shahramian, R Behzadmehr, M Afshari… - … journal of hematology …, 2018 - ncbi.nlm.nih.gov
Background: Cholelithiasis and its predisposing factors are less characterized in
thalassemia syndromes. In the present study, we assessed the prevalence of gallstones and …

Genetic epidemiology and functional studies of β-thalassaemia in Kilifi, Kenya

AW Macharia - 2023 - search.proquest.com
It is generally believed that β-thalassaemia is rare in sub-Saharan Africa; however, in
studies conducted in Kilifi, we recently observed HbA2 levels within the diagnostic range for …

Spectrum of β-thalassemia mutations in some areas of Guangxi Zhuang autonomous region of Southern China: a study on a pediatric population aged 0–15 years

LF Huang, LL Yu, L Nikuze, S Singh, JX Jiang… - …, 2021 - Taylor & Francis
Abstract β-Thalassemia (β-thal), one of the most common form of single-gene inheritable
blood diseases in the world, is highly prevalent in southern China, especially in the Guangxi …

Prenatal diagnosis of the hemoglobinopathies

JM Old - Genetic Disorders and the Fetus: Diagnosis …, 2015 - Wiley Online Library
Numerous PCR‐based techniques can be used to diagnose the globin gene mutations, this
chapter compares and contrasts these different approaches to diagnose the …

[HTML][HTML] Novel insight into intellectual disability; A review article

N Parsamanesh, E Miri-Moghaddam - Gene, Cell and Tissue, 2018 - brieflands.com
: Intellectual disability or cognitive disturbance is a prevalent neurological problem
determined by the low-level intelligence quotient (< 70). Intellectual disability affects …

Carrier screening for the haemoglobinopathies: past, present and future

J Old, C Harteveld - OBM Genetics, 2017 - lidsen.com
Carrier screening for the haemoglobinopathies has undergone many technological
improvements in haematological and molecular diagnostic techniques since the first …

Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients

S AbdulAzeez, NB Almandil, ZA Naserullah… - Molecular Biology …, 2020 - Springer
In the Eastern province of Saudi Arabia, thalassemia is highly common. Data on the effect of
alpha globin gene variation on the concentration of iron on transfusion dependent Saudis …