What is thalassemia?

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Multiple Choice

What is thalassemia?

Explanation:
Thalassemia is a genetic disorder that impacts the body's ability to produce hemoglobin, which is a critical component of red blood cells responsible for transporting oxygen throughout the body. This condition is characterized by an imbalance in the production of alpha or beta globin chains that make up hemoglobin. As a result, individuals with thalassemia may experience anemia, fatigue, weakness, and other health complications due to insufficient hemoglobin levels or abnormal hemoglobin production. The disorder is inherited in an autosomal recessive manner, meaning that a child must receive a defective gene from both parents to exhibit symptoms of the disease. Understanding thalassemia as a genetic disorder emphasizes the significance of genetic factors in hematologic health and the potential need for genetic counseling in affected families.

Thalassemia is a genetic disorder that impacts the body's ability to produce hemoglobin, which is a critical component of red blood cells responsible for transporting oxygen throughout the body. This condition is characterized by an imbalance in the production of alpha or beta globin chains that make up hemoglobin. As a result, individuals with thalassemia may experience anemia, fatigue, weakness, and other health complications due to insufficient hemoglobin levels or abnormal hemoglobin production. The disorder is inherited in an autosomal recessive manner, meaning that a child must receive a defective gene from both parents to exhibit symptoms of the disease. Understanding thalassemia as a genetic disorder emphasizes the significance of genetic factors in hematologic health and the potential need for genetic counseling in affected families.

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