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View Nurseslabs Sickle Cell Anemia Images. Sickle cell anemia, or sickle cell disease (scd), is a genetic disease of the red blood cells (rbcs). Normally, rbcs are shaped like discs, which gives them the flexibility to travel through even the smallest blood vessels.

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Symptoms of sickle cell anemia include bacterial infections, arthritis, leg ulcers, fatigue, and lung and heart injury. This change in shape prevents red blood. Sickle cell anemia is a disease passed down through families in which red blood cells form an abnormal sickle or crescent shape.

The most common type is known as sickle cell anaemia (sca).

This change in shape prevents red blood. Hemoglobin ss disease (hb ss); This gene causes the hemoglobin molecule to be defective. Anemia is a condition in which the hemoglobin concentration is lower than normal.

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Homozygous sickle cell anemia (hbss, autosomal recessive) is the most common variant of the sickle cell syndromes and occurs predominantly in individuals of african and east mediterranean descent.

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Lastly, sickle cell anemia provides an outstanding opportunity to build a connection between genetics and evolution.

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In order for full disease symptoms to manifest in an individual they must carry two copies (homozygous genotype = ss) of the hbs gene.

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The sickle cells also get stuck in blood vessels, blocking blood flow.1 signs and symptoms of sickle cell disease usually begin in early childhood and may include anemia, repeated infections, and periodic episodes of pain (called crises).

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Anemia is a condition in which the hemoglobin concentration is lower than normal.

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Sickle cell anemia is an inherited blood disorder that causes red blood cells, which are normally round and flexible, to become stiff and crescent shaped.

Source: www.wikidoc.org

Sickle cell anemia, or sickle cell disease (scd), is a genetic disease of the red blood cells (rbcs).

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The most common type is known as sickle cell anaemia (sca).

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