0
What else can I help you with?
What is the Life span for hemoglobin SC disease or hemoglobin S beta thalassemia?
4 months
Can person that have hemoglobin e trait marry with a beta thalassemia carrier?
Yes, a person with hemoglobin E trait can marry a beta thalassemia carrier. However, it is important for both individuals to undergo genetic counseling to understand the potential risks for their children. They could have offspring with various combinations of hemoglobin disorders, including hemoglobin E disease or beta thalassemia. Genetic testing can help assess the likelihood of these outcomes.
What is thalesemmia entermedia?
Thalassemia Intermedia is a recessive trait inherited disease of the red blood cells. In thalassemia, the genetic defect results in reduced rate of synthesis of normal hemoglobin chains.
Is thalassemia a type of blood cancer?
No, thalassemia is not a type of blood cancer. It is an inherited blood disorder that affects the production of hemoglobin, which can lead to anemia and other complications. Blood cancers, such as leukemia, lymphoma, and myeloma, involve the uncontrolled growth of abnormal blood cells.
Which system is related with thelesemia disease?
The thalassemia disease is related to the hematological system, specifically affecting the production of hemoglobin in the blood. Thalassemia results in the body's inability to produce enough healthy red blood cells, leading to anemia and other complications.
What is a hemoglobin doctor called?
A doctor who specializes in diseases and disorders related to hemoglobin is typically called a hematologist. Hematologists have expertise in diagnosing and treating conditions such as anemia, sickle cell disease, and thalassemia that affect the production and function of hemoglobin in the body.
Is thalassemia a type of cancer?
Thalassemia is an autosmal recessive blood disease. That means that it is an inherited disease. Thalassemia in more common in Mediteranian people.
Can mild thalassemia be a major thalassemia?
No. A minor form of the blood disorder thalassemia is when you inherited just one beta thalassemia gene, along with a normal beta-chain gene. This manifests as mild anaemia with a slight lowering of the hemoglobin level in the blood. No treatment is require. By contrast, a thalassemia major, also known as Cooley's Disease, is when one is born with two genes for beta thalassemia and no normal beta-chain gene. This is a serious disorder.
What is the test detects abnormal hemoglobin molecule?
The test that detects abnormal hemoglobin molecules is called hemoglobin electrophoresis. This laboratory technique separates different types of hemoglobin based on their electrical charge and size, allowing for the identification of various hemoglobin variants, such as those found in conditions like sickle cell disease or thalassemia. It is commonly used to diagnose and monitor hemoglobinopathies.
What are the different types of sickle cell disease and how do they differ from each other?
There are several types of sickle cell disease, including sickle cell anemia, sickle beta thalassemia, and sickle cell-hemoglobin C disease. These types differ based on the specific genetic mutations that affect the hemoglobin protein in red blood cells. Sickle cell anemia is the most common and severe form, where individuals have two copies of the sickle cell gene. Sickle beta thalassemia and sickle cell-hemoglobin C disease are milder forms that result from different combinations of genetic mutations. Symptoms and complications can vary among the different types of sickle cell disease.
What is hgb hic?
HGB HIC, or Hemoglobin H Disease, is a type of thalassemia, specifically an alpha-thalassemia disorder. It occurs when there is a deficiency in the production of alpha globin chains, leading to an excess of beta globin chains that form unstable hemoglobin (Hemoglobin H). This condition can result in moderate to severe anemia, fatigue, and other health complications. Management typically involves regular monitoring and supportive care, and in some cases, blood transfusions may be necessary.
Are there other names for Thalassemia disease?
Alpha thalassemia silent carrierAlpha thalassemia minor, also called alpha thalassemia traitHemoglobin H diseaseAlpha thalassemia major, also called hydrops fetalisBeta thalassemia minor, also called beta thalassemia traitBeta thalassemia intermediaBeta thalassemia major, also called Cooley's anemia or beta-zero (ß0) thalassemiaBeta-plus (ß+) thalassemiaMediterranean anemia
