What is thalassemia?

 * What is thalassemia? *

Anemia is an inherited disease in which the human body does not produce enough blood to meet its needs and the body makes an abnormal form of hemoglobin. Hemoglobin is a protein found in the blood that Sends oxygen from one place to another.

This causes the destruction of red blood cells and leads to anemia. Anemia is a disease in which I do not have normal and healthy red blood cells.

Thalassemia medication is one of the most dangerous types.

The first alpha thalassemia involves a change in the alpha globin genes. To make alpha globin, you need four parents, take two genes from each parent. And another beta-thalassemia in which beta-globin genes are mutated. Two genes, one in every parent, are inherited to make beta-globin.

Thalassemia minor careers are medically cured. If both men and women have thalassemia minor careers and they both get married, the children that will be born to them are called thalassemia major children and it causes trouble for parents and children.

Symptoms:

  • * Changes in the bones, especially the face
  • * Black urine
  • * Decrease in development and growth
  • * Fatigue and lethargy
  • * Yellowing of the skin

Causes:

  • * Thalassemia is caused by a change in the gene that produces hemoglobin and can also be passed on to parents.
  • * Thalassemia is the most reliable source of people in Asia, the Middle East, Africa, and the Mediterranean, such as Greece and Turkey.

Treatment:

  • * Blood test
  • * Hemoglobin test
  • * Genetic tests

 

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