HBB gene. The Nemours Foundation. Beta thalassemia (for parents). Fibach E, Rachmilewitz EA. Pathophysiology and treatment of patients with beta-thalassemia - an update. F1000Res. 2017;6:2156.

This causes symptoms that are moderate to severe ... You get one from each parent. Subtypes of beta thalassemia include: Beta thalassemia minima, in which you have one missing or mutated gene ...

Beta thalassemia is a blood condition that causes low levels of functional red blood cells. Inherited mutations in the HBB gene cause it. The HBB gene gives your body instructions for producing ...

Sickle cell beta-thalassemia refers to an inherited condition that impacts hemoglobin. People with the condition have different changes in each copy of their hemoglobin gene. One causes red blood ...

Beta-thalassemia, also known as β-thalassemia ... of iron could negatively affect mitochondrial function, worsening the pathophysiology of the disease. The buildup of iron in mitochondria may ...

Beta thalassemia is a condition in which the body doesn’t make enough hemoglobin, the oxygen-carrying molecule in blood. It causes a person to be anemic, which makes them to feel weak ...

Most healthy hemoglobin includes two proteins: alpha-globin and two beta-globin. Inheriting faulty alpha-globin genes causes alpha-thalassemia. Likewise, inheriting faulty beta-globin genes ...

You most likely have beta thalassemia minor (one normal gene and one that causes low beta-cell-chain production), which consists of mild anemia and very small cells. This condition can look very ...

Commonly known types of SCD include Haemoglobin SS, Haemoglobin SC, and Haemoglobin beta thalassemia. Causes Symptoms Symptoms of sickle cell disease include – Also Read: Stop smelly fart ...

Anemia from "beta thalassemia intermedia" causes slowed growth in children, weak bones, and an enlarged spleen. "Beta thalassemia major" is the most serious type, and it can cause many ...