What is the anemia of Thalassymia?

Thalassymia anemia is a recessive genetic state that occurs in people of Mediterranean origin. The large family of related conditions is known together as thalassemia and these conditions can have a number of forms. In some regions where these conditions are endemic, governments strongly recommended blood testing to identify carriers and make thalassemia anemia less common and to identify cases at the beginning of pregnancy to provide appropriate supporting care. There are three types, each named after the type of globin chain: alpha, beta and delta thalassemia. Because this feature is recessive, people with only one copy of a defective gene usually experience mild anemia or no symptoms, while people with both copies have more serious symptoms. Hemoglobin H or Alfa Minor is an associated with hemolytic anemia in which blood cells disintegrate in response to various environmental triggers, causing anemia. Medicines and food treatment can be treated. Alpha Major is usually incompatible withLife: People who were born with this condition die shortly after birth, not if before.

beta thalassemie, the most common form, also has a main and smaller variant. A smaller variant usually causes minimal symptoms, while the main version, also known as Cooley anemia, can be treated with blood transfusions to increase hemoglobin, along with medicines that help the body express iron so that iron does not threaten in the body. These conditions are very manageable if patients remain at the top of their regime.

delta thalassymia is closely related to beta thalassymia anemia and usually causes little symptoms in the patient. However, people can have a beta and delta thalassymia and the presence of a delta form can cover a beta form that can lead to complications in correct diagnosis and treatment. For this reason, it is sometimes recommended for further testing for people with Delta Thalassemia anemia to make pIt has been reversed that they do not have a more problematic beta form.

In addition to being found in people of Mediterranean origin, Thalassymia anemia also occurs in regions where malaria is endemic. This type of anemia grants some resistance to malaria infection, which explains why the property persists for so long. People who are curious about whether they are carriers can ask for blood or genetic tests to check anemia or problem with a problem.