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How is the sickle cell disease inherited?

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How is the sickle cell disease inherited?

Sickle cell gene is inherited from both the parents. 1 set from mother and 1 set from father. This usually happens when both parents are "carriers" of the sickle cell gene, also known as having the sickle cell trait.

Last updated on 12 Dec 2024

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Related Questions

What is sickle cell anaemia?

Sickle cell anemia 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 12 Dec 2024

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How will you know if you are a carrier of sickle cell trait?

The only way to find out if you are the carrier of sickle cell anemia is to get a simple blood test done. The blood test will tell you whether you have sickle cell gene or not.

Last updated on 12 Dec 2024

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What are some characteristics of sickle cell disease?

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 12 Dec 2024

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How is the sickle cell disease inherited?

Sickle cell gene is inherited from both the parents. 1 set from mother and 1 set from father. This usually happens when both parents are "carriers" of the sickle cell gene, also known as having the sickle cell trait.

Last updated on 12 Dec 2024

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How is sickle cell anemia codominant?

Sickle cell anemia is a disease where red blood cells become thin and elongated. If a person has one copy of the sickle cell allele, half of their red blood cells will be misshapen. In this way, the allele is codominant, since both normal and sickled shapes are seen in the blood.

Last updated on 12 Dec 2024

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