Delta-beta thalassemia

Delta-beta thalassemia is a form of thalassemia, a group of inherited blood disorders that affect the body's ability to produce hemoglobin and red blood cells. Delta-beta thalassemia is caused by mutations in the HBB gene and is inherited in an autosomal recessive manner.

Symptoms

The symptoms of delta-beta thalassemia can vary greatly from person to person. Some people may have no symptoms or only mild anemia, while others may have severe anemia and other health problems. Symptoms can include fatigue, weakness, pale skin, and shortness of breath.

Causes

Delta-beta thalassemia is caused by mutations in the HBB gene. This gene provides instructions for making a protein called beta-globin, which is a component of hemoglobin. Mutations in the HBB gene disrupt the normal production of hemoglobin, leading to a shortage of red blood cells and anemia.

Diagnosis

Delta-beta thalassemia is diagnosed through a combination of blood tests, genetic testing, and sometimes bone marrow examination. Blood tests can reveal anemia and abnormal hemoglobin. Genetic testing can identify mutations in the HBB gene.

Treatment

There is currently no cure for delta-beta thalassemia. Treatment is aimed at managing symptoms and preventing complications. This can include regular blood transfusions, iron chelation therapy to remove excess iron from the body, and other supportive treatments.

Prognosis

The prognosis for individuals with delta-beta thalassemia varies depending on the severity of the condition. Some people may have a normal lifespan with no symptoms, while others may have severe anemia and other health problems that can affect their quality of life.

See also

• Alpha thalassemia
• Beta thalassemia
• Hemoglobinopathy
• Sickle cell disease

Delta-beta thalassemia Resources
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