Search results
20 sie 2024 · Sickle cell disease is a genetic disorder caused by mutations in hemoglobin genes, leading to a faulty hemoglobin protein, called hemoglobin S. Hemoglobin S changes flexible red blood cells into rigid, sickle-shaped cells that can block blood flow and cause pain and organ damage.
- Diagnosis
Similar tests can also look for other abnormal hemoglobin...
- Sickle Cell Trait
People with sickle cell trait have only one copy of the...
- Pregnancy, Reproduction, and Sickle Cell Disease
Sickle cell disease can affect sexual organs and other parts...
- How Sickle Cell Disease May Affect Your Health
Sickle cell disease can cause pain, infections, and joint...
- Treatment
Transplant failure, which causes sickle cell disease to...
- Symptoms
Sickle cell disease is an inherited disease, which means you...
- Research
NHLBI-funded scientists found an effective sickle cell...
- What Is Sickle Cell Disease?
Sickle cell disease is an inherited blood disorder that...
- Diagnosis
22 gru 2022 · Sickle cell anemia is an inherited disorder that affects the shape and function of red blood cells. It is caused by a gene mutation that changes hemoglobin, the protein that carries oxygen in red blood cells. Learn more about the symptoms, risk factors and complications of this disease.
3 sie 2023 · Sickle cell disease is a genetic disorder that affects the hemoglobin in red blood cells, causing them to become sickle shaped and block blood flow. Learn about the different types of sickle cell disease, how they are inherited, and how they can be treated.
9 wrz 2023 · Causes. SCD is primarily caused by a genetic mutation affecting hemoglobin, the protein responsible for carrying oxygen in red blood cells. The underlying cause of SCD lies in a point mutation in the HBB on chromosome 11, resulting in the production of abnormal hemoglobin known as HbS.
7 maj 2019 · Sickle cell disease (SCD) is a monogenetic disorder due to a single base-pair point mutation in the β-globin gene resulting in the substitution of the amino acid valine for glutamic acid in the β-globin chain. Phenotypic variation in the clinical presentation and disease outcome is a characteristic feature of the disorder.
Sickle cell disease (SCD), also simply called sickle cell, is a group of hemoglobin-related blood disorders typically inherited. [2] The most common type is known as sickle cell anemia. [2] It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. [2]
30 wrz 2024 · Sickle cell disease is an inherited blood disorder that affects hemoglobin, the protein that carries oxygen through the body. Misshapen red blood cells can block blood flow causing lifelong health problems.
