Introduction In Pakistan, the reported carrier rate of thalassaemia is estimated to be 5%–8% with 5000 new patients diagnosed every year. Several known systemic complications of beta thalassaemia major have been studied, but no studies are conducted to assess ocular complications among these patients from our population.Methods It was a cross-sectional study design conducted at three private and public sector centres in Pakistan. We recruited 203, 11–17 years old children with beta thalassaemia major in our study. Frequency of overall ocular complications such as retinal pigment epithelium degeneration, visual field defects, increased retinal vascular tortuosity, lenticular opacities, anterior segment abnormality, etc among beta thalassaemi...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Abstract:Background: Major thalassemia is the most inherited hemoglobinopathy that caused severe and...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Background: Beta thalassemia (β-thalassemia) is a hereditary disease caused by defective globin syn...
Background: Thalassemia is a globally prevalent genetic disorder. Patients with thalassemia are pron...
Background:Purpose of current study was to study the ocular manifestations in beta-thalassemia major...
Purpose: To study the ocular manifestations in multiple transfused beta-thalassemia major patients ...
In this survey, we examined the associated complications and conditions of the patients suffering wi...
OBJECTIVES: Despite the correct application of blood transfusions and chelation treatments, beta ...
ABSTRACT Purpose: Beta-thalassemia minor, a common hereditary blood disorder in Mediterranean count...
Introduction: The current article mainly attempts to evaluate the incidences of ocular toxicity and ...
To determine and compare ocular characteristics and refractive errors between major thalassemia pati...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Background: The aim of current study was exploring the ocular abnormalities in individuals with Type...
Thalassaemic patients with diabetes mellitus are at risk of developing retinopathy. To evaluate the ...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Abstract:Background: Major thalassemia is the most inherited hemoglobinopathy that caused severe and...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Background: Beta thalassemia (β-thalassemia) is a hereditary disease caused by defective globin syn...
Background: Thalassemia is a globally prevalent genetic disorder. Patients with thalassemia are pron...
Background:Purpose of current study was to study the ocular manifestations in beta-thalassemia major...
Purpose: To study the ocular manifestations in multiple transfused beta-thalassemia major patients ...
In this survey, we examined the associated complications and conditions of the patients suffering wi...
OBJECTIVES: Despite the correct application of blood transfusions and chelation treatments, beta ...
ABSTRACT Purpose: Beta-thalassemia minor, a common hereditary blood disorder in Mediterranean count...
Introduction: The current article mainly attempts to evaluate the incidences of ocular toxicity and ...
To determine and compare ocular characteristics and refractive errors between major thalassemia pati...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Background: The aim of current study was exploring the ocular abnormalities in individuals with Type...
Thalassaemic patients with diabetes mellitus are at risk of developing retinopathy. To evaluate the ...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Abstract:Background: Major thalassemia is the most inherited hemoglobinopathy that caused severe and...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...