Deletions or mutations in the genes that make hemoglobin mean that your red blood cells might form ... and β globin chains, different mutations result in either alpha- or beta-thalassemia.

It is a genetic blood disorder that affects the production of hemoglobin, which is made of two types of protein chains -- alpha globin and beta ... thalassemia," says the expert Alpha thalassemia ...

World Thalassemia Day was observed on 8 May. India records between 10,000 and 15,000 new cases of Thalassemia Major every ...

People with hemoglobin H, a form of alpha ... specific type of thalassemia a person has is typically due to inherited factors. Four alpha-globin and two beta-globin protein chains make up hemoglobin.

Mainly, thalassemia disease is of two types: Alpha and Beta thalassemia disease ... Four globin genes are required to make beta-globin chains, one from each parent. C. Beta thalassemia is common ...

Alpha-thalassemia is one of the most common hemoglobin genetic abnormalities and is caused by the reduced or absent production of the alpha globin chains. Alpha-thalassemia is prevalent in ...

Though the treatments for beta thalassemia are similar to those for sickle cell disease, the condition has a different cause. Hemoglobin has two parts, an alpha chain and a beta chain. In beta ...

It normally has two alpha chains and two beta chains ... However, the anemia is less severe. Hemoglobin SB+ (beta) thalassemia affects beta globin gene production. The size of the red blood ...

DEAR DR. ROACH: I am Greek and have thalassemia minor ... very common in the Mediterranean.) Alpha thalassemias have reduced or missing alpha chains, while beta thalassemias have reduced or ...

Beta thalassemia major is the most severe type. The alpha form occurs when there is an alteration in genes related to the alpha globin protein while the beta form is related to similar genes ...

Alpha thalassemia minor affects the alpha hemoglobin chain, and beta thalassemia minor, naturally enough, affects the beta chain. Alpha thalassemia minor is a mild disease, usually noted by ...

for the treatment of adult patients with non-transfusion-dependent and transfusion-dependent alpha- or beta-thalassemia. The review classification for this application is Standard and the ...