Hemoglobinopathy

Hemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule. Hemoglobinopathies are inherited single-gene disorders; in most cases, they are inherited as autosomal co-dominant traits.

Overview

Hemoglobinopathies are often considered as a group, including thalassemia and sickle cell disease. They are common genetic disorders in the world, particularly in people of African, Mediterranean, and Southeast Asian ancestry.

Types of Hemoglobinopathy

There are many types of hemoglobinopathy, the most common of which are:

• Beta thalassemia - This is caused by reduced (beta+) or absent (beta0) synthesis of the beta globin chains of hemoglobin.
• Alpha thalassemia - This is caused by reduced (alpha+) or absent (alpha0) synthesis of the alpha globin chains of hemoglobin.
• Sickle cell disease - This is caused by a mutation in the HBB gene on chromosome 11. It is inherited in an autosomal recessive manner.

Symptoms

The symptoms of hemoglobinopathy can vary greatly depending on the specific type of disorder. Some people may have no symptoms or mild anemia, while others may have severe symptoms. Common symptoms can include:

• Fatigue and weakness
• Pale or yellowish skin
• Abdominal pain
• Dark urine
• Delayed growth and development in children
• Shortness of breath

Diagnosis

Hemoglobinopathies are diagnosed through blood tests that look for abnormal hemoglobin molecules. These tests can include:

• Complete blood count (CBC)
• Hemoglobin electrophoresis
• Genetic testing

Treatment

Treatment for hemoglobinopathies is aimed at managing symptoms and avoiding complications. This can include:

• Regular blood transfusions
• Medications to reduce pain and prevent complications
• Bone marrow transplant

See Also

• Anemia
• Genetic disorder
• Blood transfusion
• Bone marrow transplant

References

Hemoglobinopathy Resources
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