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How does sickle cell trait differ from sickle cell disease People with sickle cell trait have inherited an abnormal gene (hemoglobin s) from one parent and a normal gene (hemoglobin a) from the other parent Sickle cell disease scd affects the form and function of your red blood cells.

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People with sickle cell trait (sct) inherit one sickle cell gene and one normal gene Hemoglobin is a protein that carries oxygen from the lungs to all parts of the body People with sct usually do not have any of the symptoms of sickle cell disease (scd), but they can pass the trait on to their children

Talk to your doctor about getting tested for sct if you are at risk.

Sickle cell trait occurs when a person carries a single gene for sickle cell disease (scd) This is estimated to affect 1 million to 3 million americans and 8 to 10 percent of african americans Sickle cell trait can also affect hispanics, south asians, caucasians from southern europe, and people from middle eastern countries More than 100 million people worldwide have sickle cell trait.

Sickle cell trait describes a condition in which a person has one abnormal allele of the hemoglobin beta gene (is heterozygous), but does not display the severe symptoms of sickle cell disease that occur in a person who has two copies of that allele (is homozygous) Those who are heterozygous for the sickle cell allele produce both normal and abnormal hemoglobin (the two alleles are. Sickle cell trait occurs when a person has one copy of the sickle cell gene passed down from one parent, and a normal hemoglobin gene from the other parent This fact sheet describes what sickle cell trait is, who is affected, how to know if you have it, and how to live well with sickle cell trait.

The sickle cell trait is passed down through families

Learn how you inherited this trait and how it differs from sickle cell disease. Sickle cell trait is a genetic feature that affects red blood cells It usually causes no symptoms, but it can increase the risk of certain health issues. Sickle cell trait is a change (mutation) in a gene that affects the hemoglobin in red blood cells

All red blood cells contain hemoglobin