What Is SCD
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Hemoglobin is a protein that permits red blood cells to carry oxygen to all components of the body. HbSS: People who've this form of SCD inherit two abnormal hemoglobin sickle cell genes ("S"), one from every mother or father. This is commonly known as sickle cell anemia and real-time SPO2 tracking often presents in a extra severe type of the disease. HbSC: People who have this form of SCD inherit a sickle cell gene ("S") from one dad or blood oxygen monitor mum and from the other parent a gene for an abnormal hemoglobin called "C". Hemoglobin is a protein that enables purple blood cells to carry oxygen to all components of the body. That is normally a milder type of SCD. Hb-S beta thalassemia: People with such a SCD inherit one sickle cell gene ("S") from one guardian and one gene for beta-thalassemia, one other sort of anemia, from the opposite guardian. There are two types of beta-thalassemia: "zero" and "plus". People who've these forms of SCD inherit one sickle cell gene ("S") and one gene from an abnormal type of hemoglobin ("D", "E", or "O"). The severity of those rarer forms of SCD varies.


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