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15 de may. de 2024 · Sickle cell trait (SCT) is when a person inherits one sickle cell gene and one normal gene. People with SCT usually do not have symptoms of sickle cell disease (SCD), but they can pass the trait on to their children and may experience some complications in certain situations.
28 de ene. de 2021 · Learn the difference between sickle cell trait and sickle cell disease, two inherited blood disorders that affect millions of people worldwide. Find out the symptoms, complications, treatments, and genetic counseling options for both conditions.
22 de ago. de 2024 · Sickle cell trait is different from sickle cell disease, which is caused by two copies of the sickle hemoglobin gene. Learn about the symptoms, screening, and inheritance of sickle cell trait.
25 de feb. de 2024 · Sickle cell trait is a genetic condition that results when an individual inherits a gene for normal hemoglobin (A) and a gene for sickle hemoglobin (S) that results in the genotype (AS). Conversely, sickle cell disease occurs when an individual inherits 2 abnormal sickle genes (SS).
6 de dic. de 2023 · Sickle cell trait is a benign carrier condition, usually with none of the symptoms of sickle cell anemia or other sickle cell diseases. However, knowledge of sickle cell trait is important in many settings, such as preconception counseling and evaluation of rare complications.
Learn about sickle cell disease, a genetic disorder that affects red blood cells and causes pain, anemia and complications. Find out the difference between sickle cell trait and disease, and how they are inherited and diagnosed.
Sickle cell disease (SCD) is the consequence of homozygosity for a single amino acid change in the β-globin chain that results in structurally abnormal hemoglobin S, or by compound heterozygosity for hemoglobin S and another β-globin chain abnormality, typically hemoglobin C or β-thalassemia.
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