Thalassemia is a blood disorder that is inherited. This means it's passed down from one or both parents through their genes. When you have thalassemia, your body makes less hemoglobin than normal. Hemoglobin is an iron-rich protein in red blood cells. It carries oxygen to all parts of the body.
There are two main types of thalassemia: alpha and beta. Different genes are affected for each type.
Thalassemia can cause mild or severe anemia. Anemia occurs when your body doesn't have enough red blood cells or hemoglobin. The severity and type of anemia depends on how many genes are affected.
Beta thalassemia is caused by changed (mutated) or missing genes. The types of the disorder are based on how severe the anemia is:
Beta thalassemia minor. This is also called beta thalassemia trait. It may cause no symptoms or only mild anemia. People with this mild form may not need treatment.
Thalassemia intermedia. This causes moderate to severe anemia. You may sometimes need transfusions and other treatment.
Beta thalassemia major (Cooley anemia). This is the most severe form. People with this condition may have life-threatening anemia. They will need regular blood transfusions and other treatment.
Many people with this disorder are given iron replacement by mistake. This happens when a lack of iron is believed to cause their anemia. Too much iron can be harmful. So it's important to get the right diagnosis. You may need to see a blood disorder specialist (hematologist).
Beta thalassemia is a genetic disease inherited from one or both parents. The only risk factor is having a family history of the disease.
Different people will have different symptoms based on which type of the disorder is inherited.
This is the most severe type of this disorder. Children born with this type will have symptoms early in life that include:
Having a poor appetite
Having many infections
Over time, more symptoms will appear, including:
Belly (abdominal) swelling
Yellowish skin (jaundice)
Without treatment, the spleen, liver, and heart become enlarged. Bones can also become thin, brittle, and deformed.
People with this condition will need frequent blood transfusions and may not live a normal life span. Iron builds up in the heart and other organs from blood transfusions. This can cause heart failure as early as the teens or early 20s.
This type can cause symptoms of moderate to severe anemia. These include:
Extreme tiredness (fatigue)
Slow or delayed growth
This type often causes no symptoms.
Beta thalassemia is most often found in people who are of Greek, Italian, African, or Asian origin. The diagnosis is most often made between ages 6 and 12.
These tests may be able to tell if you are a carrier and can pass the disorder on to your children:
Complete blood count (CBC). This test checks the size, number, and maturity of different blood cells in a set volume of blood.
Hemoglobin electrophoresis. This lab test differentiates the types of hemoglobin.
All of these studies can be done from a single blood sample. In a pregnant woman, the baby is diagnosed using CVS (chorionic villus sampling) or amniocentesis.
Treatment will depend on your symptoms, age, and general health. It will also depend on how severe the condition is.
Treatment may include:
Regular blood transfusions
Medicines to reduce extra iron from your body (called iron chelation therapy)
Surgery to remove the spleen, if needed
Daily folic acid
Surgery to remove the gallbladder
Regular checks of heart and liver function
Bone marrow transplant
Do not take any iron supplements.
Complications of beta thalassemia vary depending on the type:
Thalassemia minor. This is mild and causes no problems. But you will be a carrier of the disorder.
Thalassemia intermedia. This type can cause problems based on the severity of the anemia. These problems include delayed growth, weak bones, and enlarged spleen.
Beta thalassemia major. This causes major problems and can result in early death. Complications may include delayed growth, bone problems causing facial changes, liver and gall bladder problems, enlarged spleen, enlarged kidneys, diabetes, hypothyroidism, and heart problems.
If you have beta thalassemia major or intermedia, living with the disorder may be challenging. Work with your healthcare provider to make a treatment plan that includes blood transfusions. Your plan may also include treatment to remove extra iron from your body (iron chelation therapy). You will also have regular blood tests and physical exams. It's important to prevent infections. Wash your hands often and stay away from others who are sick. You may also need emotional support. Talk with your provider. They can help you find support.
Thalassemia is an inherited blood disorder. It causes the body to make less hemoglobin.
There are several types of beta thalassemia.
Different people will have different symptoms based on which type of beta thalassemia is inherited.
Treatment of beta thalassemia may include medicines and regular blood transfusions.
Work with your healthcare provider to stay healthy and reduce complications of the disease.
Tips to help you get the most from a visit to your healthcare provider:
Know the reason for your visit and what you want to happen.
Before your visit, write down questions you want answered.
Bring someone with you to help you ask questions and remember what your provider tells you.
At the visit, write down the name of a new diagnosis and any new medicines, treatments, or tests. Also write down any new instructions your provider gives you.
Know why a new medicine or treatment is prescribed and how it will help you. Also know what the side effects are.
Ask if your condition can be treated in other ways.
Know why a test or procedure is recommended and what the results could mean.
Know what to expect if you do not take the medicine or have the test or procedure.
If you have a follow-up appointment, write down the date, time, and purpose for that visit.
Know how you can contact your provider if you have questions.