Thalassemia
Also known as: alpha-thalassemia, beta-thalassemia.
Thalassemia
Thalassemia is a blood disorder in which the body produces hemoglobin that doesn’t function properly.
Hemoglobin is the protein that carries oxygen throughout the body. Most of the protein is in red blood cells and it gives the cells and the blood, its red color. In thalassemia, the abnormal hemoglobin causes red blood cells to be deformed so they are destroyed easily. This process is called hemolysis and leads to anemia because of poor production and increased cell destruction.
What causes thalassemia?
Thalassemia is an inherited disorder, meaning, it is passed down from parents to children.
What are the symptoms of thalassemia?
Symptoms of thalassemia can include:
- jaundice
- paleness
- poor appetite
- trouble with growth
- fussiness
- frequent infections
- enlarged liver and spleen
Other complications include
gall stones and later iron overload in the liver, skin and heart.
What are thalassemia care options?
Supportive care for children with thalassemia often comes in the form of regular blood transfusions, and folate supplements. A bone marrow transplant is the only cure for those patients, as long as it is done early in life, before development of complications.
Reviewed by: Kamar Godder, MD
This page was last updated on: December 18, 2020 04:59 PM
Learn more about
Alpha Thalassemia
Alpha thalassemia is an abnormality in the production of alpha chains which causes the red cells to more easily breakdown.
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Beta Thalassemia
Beta thalassemia impacts two different types of genes. When these genes are damaged or missing, it can cause beta thalassemia.
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Sickle Beta 0 Thalassemia
Sickle cell causes the body’s hemoglobin, or red blood cells, to take on a sickle shape and not flow through the blood vessels as smoothly. The “zero” indicates that the blood has no normal hemoglobin.
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Hgb E/B 0 Thalassemia
When someone has both abnormal hemoglobin and thalassemia, one possibility is that they have Hgb E/B 0 thalassemia.
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