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Alpha thalassemia abnormal morphogenesis
Alpha Thalassemia- Abnormal Morphogensis is a group of blood disorders that affect the way the body makes hemoglobin. Hemoglobin is a protein found in red blood cells that carries oxygen throughout the body. It's made up of alpha globin and beta globin. Normally each person has four genes for alpha globin, Alpha thalassemia happens when on or more of the genes that control the making of alpha globin is absent or defective. It can cause anemia ranging from mild to severe. Also causing Genital abnormalities and terminal transverse limb defectiveness which is why it is called abnormal morphogenesis. This is most commonly found in people of African, Middle Eastern, Chinese, Southeast Asian and occasionally, Mediterranean descent.
== Thalassemia ==
Thalassemia is an inherited condition. It's carried in the genes and passed on from parents to children. People who are carriers of a thalassemia gene show no thalassemia symptoms and might not even know they are carriers. If both parents are carriers they can pass the disease to their kids. Thalassemia is not contagious.
While there are many different types of thalassemia the main two are alpha and beta.
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