Alpha Thalassemia Center - Dayton, OHDayton Hematologist Doctors for Alpha ThalassemiaType of Physician: Hematologist What is a Hematologist? A subspecialty certification by the Board of Internal Medicine or Pathology; Hematologists treat diseases of the blood, spleen, and lymph glands such as anemia, clotting disorders, sickle cell disease, hemophilia, leukemia, and lymphoma. They perform special types of transfusions and biopsy the bone marrow for analysis. Specialty: Hematology Common Name: Blood Doctor Hematologist Doctors in Dayton * Lebanon Hematology Oncology  UC College of Medicine Barrett Cancer Center  OSU Comprehensive Cancer Center Gastrointestinal Cancer  OSU Comprehensive Cancer Center Gastrointestinal Cancer  OSU Medical Center Pathology  OSU Internal Medicine  OSU Hematology & Oncology  OSU Hematology & Oncology  BV Regional Health Center Dayton, OhioUpcoming Local Events2012-05-19
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Alpha and Beta ThalassemiaRead the Alpha and Beta Thalassemia article » What are thalassemias?Thalassemias (thal-a-SE-me-ahs) are inherited blood disorders. "Inherited" means they're passed on from parents to children through genes. Thalassemias cause the body to make fewer healthy red blood cells and less hemoglobin (HEE-muh-glow-bin) than normal. Hemoglobin is an iron-rich protein in red blood cells. It carries oxygen to all parts of the body. It also carries carbon dioxide (a waste gas) from the body to the lungs, where it's exhaled. People who have thalassemias can have mild or severe anemia (uh-NEE-me-uh). This condition is caused by a lower than normal number of red blood cells or not enough hemoglobin in the red blood cells.
What Causes Thalassemias?Your body makes three types of blood cells: red blood cells, white blood cells, and platelets (PLATE-lets). Red blood cells contain hemoglobin, an iron-rich protein that carries oxygen from your lungs to all parts of your body. Hemoglobin also carries carbon dioxide (a waste gas) from your body to your lungs to be exhaled. Hemoglobin has two kinds of protein chains: alpha globin and beta globin. If your body doesn't make enough of these protein chains, red blood cells don't form properly and can't carry enough oxygen. Your body won't work well if your red blood cells don't make enough healthy hemoglobin. Genes control how the body makes hemoglobin protein chains. When these genes are missing or altered, thalassemias occur. Thalassemias are inherited disorders. That is, they're passed on from parents to their children through genes. People who get abnormal hemoglobin genes from one parent but normal genes from the other are called carriers. Carriers often have no signs of illness other than mild anemia. However, they can pass the abnormal genes on to their children. People with moderate to severe forms of thalassemia have inherited abnormal genes from... Recommended Reading Related to Alpha ThalassemiaHeart attack facts
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Anemia
- Anemia is the condition of having less than the normal number of red blood cells or less than the normal quantity of hemoglobin in the blood. The oxygen-carrying capacity of the blood is, therefore, decreased. Symptoms of anemia may include fatigue, malaise, hair loss, palpitations, and more. Treatment for anemia includes treating the underlying cause for the condition. Iron supplements, vitamin B12 injections, and certain medications may also be necessary.
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Gallstones
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Arrhythmia
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Heart Attack
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Enlarged Spleen (Splenomegaly)
- The spleen enlarges if it is asked to do excessive work in filtering or manufacturing blood cells, if there is abnormal blood flow to it, or if it is invaded with abnormal cells or deposits. Symptoms of an enlarged spleen may include weakness and fatigue, easy bleeding, and poor white blood cell function. Treatment of an enlarged spleen is focused toward the cause of the splenomegaly. Surgery may be required to remove the spleen.
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Jaundice
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Malaria
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Abnormal Heart Rhythms (Heart Rhythm Disorders)
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Heart Disease
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Sickle Cell Disease (Sickle Cell Anemia)
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Puberty
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Beta Thalassemia
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G6PD Deficiency
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Pregnancy Planning
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Genetic Counseling
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