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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]
Niedokrwistość sierpowata, anemia sierpowata (łac. anaemia drepanocytica, ang. sickle cell anemia) – rodzaj wrodzonej niedokrwistości spowodowanej nieprawidłową budową hemoglobiny.
22 gru 2022 · Sickle cell anemia is a genetic disorder that affects red blood cells, causing pain, anemia, infections and organ damage. Learn about the symptoms, causes, risk factors, complications and prevention of this disease from Mayo Clinic.
30 wrz 2024 · Sickle cell disease is a group of inherited disorders that affect hemoglobin, the protein that carries oxygen in red blood cells. Learn about the causes, symptoms, complications, and treatments of this lifelong illness, and the NHLBI's research and clinical progress toward cures.
4 wrz 2023 · Sickle cell anemia is an inherited disorder of the globin chains that causes hemolysis and chronic organ damage. Sickle cell anemia is the most common form of sickle cell disease (SCD), with a lifelong affliction of hemolytic anemia requiring blood transfusions, pain crises, and organ damage.
21 sie 2024 · Learn about sickle cell anemia, a severe inherited blood disorder that affects red blood cells and causes anemia, pain and infections. Find out how it's diagnosed, treated and prevented, and what complications it can cause.
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.
