Thalassemia is an autosmal recessive blood disease. That means that it is an inherited disease. Thalassemia in more common in Mediteranian people.
Thalassemia affects the blood and specifically impacts the body's ability to produce hemoglobin, the protein in red blood cells that carries oxygen. This genetic condition results in abnormal hemoglobin production, leading to anemia and potential complications.
One type of red blood cell disorder is sickle cell anemia, a genetic condition in which red blood cells become rigid and sticky, leading to blockages in blood vessels and reduced oxygen delivery to tissues.
Individuals with type A positive blood have the benefit of being able to receive blood transfusions from donors with type A or type O positive blood. This blood type is also associated with a lower risk of heart disease and certain types of cancer. Additionally, individuals with type A positive blood may have a reduced risk of developing severe malaria.
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.
Yes, certain diseases are tied to blood type. This does not mean that if you have a certain blood type that you will develop these diseases. It does, however, mean that you are likely at a somewhat increased risk due to your blood type.
Thalassemia is an autosmal recessive blood disease. That means that it is an inherited disease. Thalassemia in more common in Mediteranian people.
No, thalassemia is a genetic blood disorder that affects the production of hemoglobin in red blood cells. Blood group and Rh factor are determined by different genetic markers and are not directly linked to thalassemia.
There are several types of Thalassemia. It's believed to have originated in the Middle East & the Mediterranean areas.
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.
If you have Thalassemia major but your boyfriend is not a carrier then the child will be born a healthy carrier (thalassemia minor) but shouldn't need blood transfusions. If your boyfriend is a carrier then you would have a 50% chance of having a child with thalassemia major like you do.
Myeloma - or a type of blood cancer. Tends to target African Americans supposedly.
Thalassemia and sickle cell anemia.
The inherited blood disorder that causes mild or severe anemia due to reduced hemoglobin and fewer red blood cells than normal is called thalassemia. Thalassemia is a genetic condition that affects the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. Treatment options for thalassemia may include blood transfusions, medication, and in some cases, bone marrow transplants.
Most probably he has beta thalassemia major, or Cooley's anemia What is the age of child ? If it is below 2 years it may be thalassemia major.
If untreated, beta thalassemia major can lead to severe lethargy, paleness, and delays in growth and development. The body attempts to compensate by producing more blood, which is made inside the bones in the marrow.
Thalassemia - which affect the red blood cells as oppose to white blood cells in leukemia.
beta thalassemia