Should thalassemia carriers marry? Can thalassemia be prevented? Doctor shares information about this blood disorder that ...

With gene therapy offering new hope for thalassemia, experts urge Indian govt to invest in early diagnosis, genetic testing, ...

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 high as ...

Types include alpha and beta thalassemia. Thalassemia may cause you to experience anemia-like symptoms that range from mild to severe. Treatment can consist of blood transfusions and iron chelation ...

The results have been published in the Journal of Genetics and Genomics. Severe thalassemia includes conditions like Hb Bart's hydrops fetalis and transfusion-dependent thalassemia (TDT), which ...

The symptoms of alpha thalassemia depend on how many genes are affected and ... However, in alpha thalassemia, especially the silent or trait forms, this test may appear normal, making it less ...

The finding is an association, not proof that ultraprocessed foods cause Parkinson’s disease, a progressive and incurable condition marked by tremors, muscle stiffness and other symptoms.

You may pass this gene to your children as a carrier, but you won't have symptoms. Alpha thalassemia minor, when you have two missing or mutated genes. You might have mild symptoms or none at all.

Agios is hoping for a broad label in thalassemia, covering both alpha and beta subtypes regardless of transfusion dependence. They estimate that this market (18+) is 6,000 in the US. Interestingly ...

But because their body can still make enough healthy hemoglobin, alpha-thalassemia trait usually won’t cause any symptoms. Inheriting three faulty alpha-globin genes causes more significant ...

Thalassemia is a hereditary disorder that affects the production of hemoglobin. Hemoglobin is the component of red blood cells that carries oxygen to the tissues of the body. There are many types of ...