Beta-thalassemia is one of a group of hereditary blood conditions that result from reduced or absent synthesis of the beta-globin chain of the hemoglobin molecule. It occurs as the result of a ...

A family of Albanian descent had an unusual form of beta thalassemia. The father of two children with mild thalassemia major had normal ... soluble alpha chains on electrophoresis of hemolysates ...

in which you have two missing or mutated genes and moderate symptoms Beta thalassemia major (Cooley's anemia), in which you have two missing or mutated genes and serious symptoms Your symptoms ...

Thalassemia is an inherited blood disease which causes defective red blood cell production leading to low haemoglobin and such patients need lifelong blood transfusions to cope up with life.

1 The presence of 2 thalassemia genes is often associated with severe hematologic disease. Homozygous β thalassemia usually produces thalassemia major, a profound, transfusion-dependent anemia.

World Thalassemia Day was observed on 8 May. India records between 10,000 and 15,000 new cases of Thalassemia Major every year, with national carrier rates estimated at 3 to 4 per cent, and as ...

Capillary Electrophoresis is one of the newer methods for the detection and evaluation of hemoglobinopathies. It improves upon the alkaline gel electrophoresis platform with a similar migration order, ...

Approximately 5,000 children are diagnosed with beta thalassemia major every year in Pakistan. When two individuals with minor thalassemia traits marry, there is a 25% chance that their child will ...

Alpha thalassemia results from defective alpha globin genes, while beta thalassemia involves mutations in beta globin genes. "Beta thalassemia major, also known as Cooley’s anemia, is often more ...

People with thalassemia trait in one gene. Parents with thalassemia genes have 25% risk of passing it, confirmed through hemoglobin electrophoresis blood tests. Symptoms ...

For beta thalassemia minor in particular, iron overload isn’t a problem, but other thalassemias can cause iron overload. So, giving iron can be harmful for some. In your case, I expect that your ...

The US Food and Drug Administration has approved a second use for the first CRISPR-based medicine, Casgevy, which was approved in December to treat sickle cell disease.