Sickle-cell anemia would be best described as a mutation of the haemoglobin gene. This is a blood disorder which is inherited in most cases.
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Sickle-cell anemia is caused by a mutation in the gene that codes for hemoglobin, a protein that helps red blood cells carry oxygen. This mutation leads to the production of abnormal hemoglobin known as hemoglobin S, which causes red blood cells to become rigid and sickle-shaped. These sickle-shaped cells can block blood flow, leading to pain, organ damage, and other complications.
Sickle cell anemia is caused by a mutation in the gene that encodes for the beta-globin chain of hemoglobin. This mutation results in the production of abnormal hemoglobin molecules (hemoglobin S), leading to the characteristic sickle shape of red blood cells.
Sickle cell anemia and thalassemia are two diseases caused by mutation of the protein hemoglobin.
Sickle cell anemia is caused by a mutation in the HBB gene, which provides instructions for making a protein called beta-globin. This mutation results in the production of abnormal hemoglobin known as hemoglobin S, which causes red blood cells to become rigid and form a characteristic sickle shape.
Yes, achondroplasia is primarily caused by a specific mutation in the FGFR3 gene. This mutation leads to abnormal bone growth and results in the characteristic features of achondroplasia, such as short stature and characteristic facial features.
Sickle cell anemia is caused by a point mutation in the HBB gene, specifically a substitution of adenine for thymine in the sixth codon of the gene, resulting in the production of abnormal hemoglobin known as hemoglobin S.