Increased HbA2 is a characteristic finding in minor beta thalassemia. Minor β-thalassemia is a heterozygote form of β-thalassemia that carries thalassemia genes but does not cause thalassemia disease. Diagnosis of carriers is done by CBC, RBC Index, and HbA2 test. Very few cases of people with minorthalassemia have a normal HbA2. According to the results of this pilot study it seams that percentage of minor thalassemia is noticeable in Kerman province. In this survey parents of thalassemia major and intermedia were evaluated. The result showed that about two percent of them had normal HbA2 . All of the people with normal HbA2 were born in Kerman. We suggest that this type of study should be done in different cities of this province in order...
Objective: Thalassemia carrier screening in siblings of thalassemia major patients by HbA2 estimatio...
The aim of present study was to report the frequency of β-Thalassemia trait and other hemoglobinopat...
Objectives: The aim of the study was to study the incidence of thalassemia minor by determining HbA2...
Level of HbA2 more than 4% is the reliable parameter to identify β- thalassemia carrier. However, in...
Abstract Background & Objectives: Thalassemia syndromes isone of the inherited disorders in which on...
Level of HbA2 more than 4% is the reliable parameter to identify β- thalassemia carrier. However, in...
A representative sample of a thousand volunteer university students was screened for eviden...
Introduction: The most effective way to prevent thalassemia is to screen for the disease at the po...
Beta thalassaemia is one of the most common inherited haemoglobinopathies, characterised by reduced ...
Objective: To determine the frequency of beta-thalassemia minor in subjects with no family history o...
"nAbstract "nIntroduction: The current study evaluated the value of red blood cell (RBC) i...
Background: Mutations in β-globin gene may result in β-thalassemia major, which is one of the most c...
Background: Hb A2 is elevated in subjects with beta thalassemia minor but small percent of carriers ...
Thalassemia minor is known to be a hereditary disease involving affected globin chains. In Thalassem...
Objective: To determine the prevalence of β thalassemia in Sindhi community of Wardha and evaluation...
Objective: Thalassemia carrier screening in siblings of thalassemia major patients by HbA2 estimatio...
The aim of present study was to report the frequency of β-Thalassemia trait and other hemoglobinopat...
Objectives: The aim of the study was to study the incidence of thalassemia minor by determining HbA2...
Level of HbA2 more than 4% is the reliable parameter to identify β- thalassemia carrier. However, in...
Abstract Background & Objectives: Thalassemia syndromes isone of the inherited disorders in which on...
Level of HbA2 more than 4% is the reliable parameter to identify β- thalassemia carrier. However, in...
A representative sample of a thousand volunteer university students was screened for eviden...
Introduction: The most effective way to prevent thalassemia is to screen for the disease at the po...
Beta thalassaemia is one of the most common inherited haemoglobinopathies, characterised by reduced ...
Objective: To determine the frequency of beta-thalassemia minor in subjects with no family history o...
"nAbstract "nIntroduction: The current study evaluated the value of red blood cell (RBC) i...
Background: Mutations in β-globin gene may result in β-thalassemia major, which is one of the most c...
Background: Hb A2 is elevated in subjects with beta thalassemia minor but small percent of carriers ...
Thalassemia minor is known to be a hereditary disease involving affected globin chains. In Thalassem...
Objective: To determine the prevalence of β thalassemia in Sindhi community of Wardha and evaluation...
Objective: Thalassemia carrier screening in siblings of thalassemia major patients by HbA2 estimatio...
The aim of present study was to report the frequency of β-Thalassemia trait and other hemoglobinopat...
Objectives: The aim of the study was to study the incidence of thalassemia minor by determining HbA2...