Alpha-Thalassemia Trait
Alpha-Thalassemia Trait is a genetic condition where a person inherits a mutation in one or two of the four alpha-globin genes. This condition often leads to mild anemia, which means the body has fewer red blood cells than normal. Many individuals with this trait may not experience any symptoms and can lead a normal life.
People with Alpha-Thalassemia Trait usually have a family history of thalassemia or related blood disorders. It is important for individuals with this trait to be aware of their genetic status, especially if they plan to have children, as it can affect offspring if both parents carry the trait.