What is Alpha Thalassemia? (Blood Disorder) - Overview, Symptoms, Causes, Treatment, and Prevention. Learn more: [ Ссылка ]

Alpha Thalassemia is a rare blood disorder that disrupts the body's production of hemoglobin. Hemoglobin is a protein that helps carry oxygen throughout the body. Alpha Thalassemia also reduces the red blood cell count in the body, which could possibly lead to Anemia. Anemia itself can lead to a host of additional symptoms and complications.

There are two types of Alpha Thalassemia: Hb Bart and HbH. Hb Bart is the more severe form of the disorder, and there is no effective treatment for it. HbH is less severe, and blood transfusions and bone marrow transplantations can be used to manage its conditions. Both forms of Alpha Thalassemia are inherited so there is no way to prevent the disorder.

Doctors usually diagnose Alpha Thalassemia before a child’s second birthday, but tests on a fetus can also be done to see whether he or she has inherited the disorder. Parents who are missing alpha globin genes are more likely to give birth to a child with Alpha Thalassemia. Families and sufferers are recommended to seek genetic counseling and support groups to help manage the disease.

In this video, we will answer “What is Alpha Thalassemia?” Viewers will learn the causes, symptoms, treatments, and outlook for sufferers of the disorder. There are plenty of support groups and genetic counseling services around the country that help people with Alpha Thalassemia live comfortably. By managing expectations and seeking proper care, those who suffer from Alpha Thalassemia can live a fulfilling life.

This video is meant for educational purposes and is not medical advice.

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