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SICKLE CELL ANEMIA

SICKLE CELL ANEMIA

What Is Sickle Cell Anemia?

Sickle Cell Anaemia is the most common form of sickle cell disease (SCD). SCD is a serious disorder in which the body makes sickle-shaped red blood cells. “Sickle-shaped” means that the red blood cells are shaped like a crescent.

Normal red blood cells are disc-shaped and look like doughnuts without holes in the centre. They move easily through the blood vessels. Red blood cells contain an iron-rich protein called haemoglobin. This protein carries oxygen from the lungs to the rest of the body.

Sickle cells contain abnormal haemoglobin called sickle hemoglobin or hemoglobin S. Sickle hemoglobin causes the cells to develop a sickle, or crescent shape. 

Sickle cells are stiff and sticky. They tend to block blood flow in the blood vessels of the limbs and organs. Blocked blood flow can cause pain and organ damage. It can also raise the risk for infection.

What Are the Types of Sickle Cell Disease?
What Causes Sickle Cell Anemia?
Who is at Risk for Sickle Cell Anemia?
What are the Signs & Symptoms?
How Is Sickle Cell Anemia Diagnosed?
How can Sickle Cell Anemia be prevented?
How is Sickle Cell Anemia Treated by Bone Marrow Transplant (BMT)?
Is bone marrow (stem cell) transplant the only treatment for sickle cell disease?
What are the benefits of bone marrow (stem cell) transplant?

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