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What is sickle cell anaemia?

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 19 May 2023

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Related Questions

What is like to be a sickle cell anemia patient?

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. 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

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What healthy food should a sickle cell patient take?

One is recommended to eat plenty of fruits and vegetables and pair them with whole grains, and protein foods (such as eggs, fish, chicken, meats, beans or tofu and nuts or seeds). Additionally focus on calcium-rich foods and beverages such as milk, yogurt, and cheese

Last updated on 19 May 2023

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What are sickle cells?

Sickle cells are red blood cells which look like sickle that cuts wheat. It is an inherited disorder which affects the oxygen carrying capacity in the body.

Last updated on 19 May 2023

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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 19 May 2023

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What does it mean to be a sickle cell carrier?

Sickle cell carrier are people those who inherit sickle cell gene and one normal gene. They usually pass on their sickle cell gene to their baby. This passing on makes them a sickle cell carrier.

Last updated on 19 May 2023

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