Abstract β‐thalassemia major is an inherited hemoglobinopathy that requires lifelong red
blood cell transfusions and iron chelation therapy to prevent complications due to iron …

Thalassemia management has reached new milestones, with new therapies promising the
dawning of a new era. However, conventional and new approaches require accessibility …

Sickle cell disease (SCD) and thalassemias are the most common monogenic diseases in
the world. The number of migrants and refugees in Europe and Turkey, in the past decade …

Beta thalassemia (β-thalassemia) is part of a group of inherited hemoglobinopathies caused
by a mutation in the beta globin gene, leading to minimal functional hemoglobin and …

Background Thalassemia is one of the most common chronic diseases, which cause many
problems for the patients, families, and health system. The aim of this study was to evaluate …

Background: Currently, half of the population displaced worldwide is children and
adolescents. Little is known on healthcare demand in underage migrants. Materials and …

Results Of the participants, 35 patients (70%) were Turkish citizens and 15 patients (30%)
were Syrian. The most common mutation in Turkish patients was found to be IVS-I-110 (G> …

Background Refugee or asylum seekers (RAS) children are at increased risk of physical,
developmental, and behavioral health issues. The aim of this study was to evaluate clinical …

Abstract β-Thalassaemia is an inherited blood disorder with serious complications.
Combining the unique advantages of DNA and magnetoelastic (ME) materials, an ME DNA …

Psychological and social support is one of the factors that promote resilience in refugee
children. Immigrant children with thalassemia have special psychosocial needs in the host …