1 What's SCD
Drew Kastner edited this page 2025-10-25 09:30:18 +00:00
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Hemoglobin is a protein that permits red blood cells to hold oxygen to all parts of the body. HbSS: People who have this form of SCD inherit two abnormal hemoglobin sickle cell genes ("S"), one from every parent. This is commonly referred to as sickle cell anemia and BloodVitals SPO2 usually presents in a extra extreme form of the illness. HbSC: People who've this form of SCD inherit a sickle cell gene ("S") from one father or BloodVitals SPO2 mother and from the other mum or dad a gene for an abnormal hemoglobin referred to as "C". Hemoglobin is a protein that enables pink blood cells to hold oxygen to all parts of the body. This is usually a milder type of SCD. Hb-S beta thalassemia: People with such a SCD inherit one sickle cell gene ("S") from one mother or father and one gene for beta-thalassemia, one other type of anemia, from the opposite mother or father. There are two types of beta-thalassemia: "zero" and "plus". People who've these types of SCD inherit one sickle cell gene ("S") and one gene from an abnormal kind of hemoglobin ("D", "E", or "O"). The severity of those rarer sorts of SCD varies.


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