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Sickle Cell?
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Complications
Inheritance
Types
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FAQ

WHAT IS SICKLE CELL ANEMIA ?

Sickle Cell anemia is a life-threatening, inherited disorder, that affects the normal functioning of the red blood cells. The major function of the red blood cell is the transportation of oxygen throughout the body. Oxygen is carried by a protein known as hemoglobin.

The normal red blood cell (picture) is usually round, flexible and capable of passing through tiny blood vessels (diagram). A sickle red blood cell (picture) when deprived of oxygen, looses it's round flexible shape and become elongated or crescent shaped, rigid and blocks blood vessels. Consequently, blocked blood vessels (diagram) leading to any organ or tissue will ultimately deprive that part of the body of blood supply.

Tissues deprived of a normal blood flow results in excruciating pain to the individual. This condition, known as Sickle Cell Crisis, cause some of the complications associated with sickle cell disorder. Quite often, the individual will require hospitalization which could average about two weeks or more. Currently, there are no cures for Sickle Cell Disorder (SCD). Remember, Sickle Cell anemia is just one type of Sickle Cell Disorder. Other known SCD is listed under Types.


[ Click here for diagram ]




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