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What is the genetic basis of sickle cell anemia?
What is the genetic basis of sickle cell anemia?
What is the genetic basis of sickle cell anemia?
Sickle cell disease (SCD) is a genetic disorder caused by a mutation in both copies of a person's HBB gene. This gene encodes a component of hemoglobin, the oxygen carrying protein in red blood cells. The mutation causes hemoglobin molecules to stick together, creating sickle-shaped red blood cells
Last updated on 19 May 2023
Related Questions
Which two blood groups produce sickle cell children?
Research hints that blood group O was the commonest blood group to pass on sickle cell anemia. However, if any of the parent was a carrier then any blood group could produce sickle cell anemia.
Last updated on 19 May 2023
What is the difference between sickle cell and blood cancer?
Both are diffrent while leukemia (blood cancer) is a type of cancer which involves uncontrolled cell division. On the contrary, sickle cell anemia is an abnormality in red blood cells. (due to lack of red blood cells).
Last updated on 19 May 2023
What are 5 symptoms of a sickle cell crisis?
The five prominent symptoms are the sickle cells die easily, vision problems, pain crisis, swelling in hands and feet and delayed growth especially during puberty.
Last updated on 19 May 2023
What are the symptoms of sickle cell anemia?
The symptoms of sickle cell anemia comprises of delayed growth, swelling on hands and feet, episodic pain, frequent infections and vision problems.
Last updated on 19 May 2023
Is jaundice a symptom of sickle cell anemia?
Yes, mild jaundice is a symptom of sickle cell anemia.
Last updated on 19 May 2023
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