A 69-year-old woman was referred to the retina service for abnormal posterior segment findings.The patient’s medical history ...

Sickle cell disease (SCD) and beta thalassaemia belong to a group of inherited conditions known as haemoglobinopathies, where the haemoglobin in red blood cells (RBCs) is affected by a genetic ...

A normal adult haemoglobin molecule (called HbA) consists of two alpha and two beta chains. Thalassemia occurs when there is a mutation or deletion in the genes that code for these globin chains.

What is alpha 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 globin. “A person normally ...

Thalassemia is an inherited blood disorder. It is passed down from one or both parents through their genes. There are two main types of thalassemia: alpha and beta. Different genes are affected for ...

However, previous studies of mouse skeletal resistance arteries found acetylcholine-stimulated vasodilation to be increased after knockdown of alpha globin gene expression. 63 We demonstrated the ...

These genes control your body's production of the two proteins that make up hemoglobin, called alpha globin and beta globin. Six genes, three from each parent, are responsible for these two proteins.

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Alpha thalassemia is inherited anemia where the body cannot produce a normal amount of hemoglobin. Hemoglobin is the protein in red blood cells that carries oxygen throughout your body. Hemoglobin A ...

The different types of thalassemia develop due to genetic mutations or deletions (where genetic code is missing) in the genes that support alpha and beta globin production.

Once the alpha globin genes were deleted, the mice experienced decreased oxygen levels comparable to individuals with severe AT.