Aplasia of the Hematopoietic Organs Endemic

Aplasia of the hematopoietic organs is a rare genetic disease that leads to disruption of the bone marrow. As a result, the level of leukocytes and platelets in the patient's blood decreases. This disease can be found in Africa, Asia, America and other regions of the world.

In most cases, this pathology occurs in children aged 4 to 7 years and is usually asymptomatic or with minor symptoms. However, in some cases, patients may experience severe forms of aplasia, which are characterized by a high degree of immune deficiency, anemia and chronic infections.

Since this pathology is associated with genetic disorders, treatment of aplasia of the hematopoietic organ is usually associated with genetic correction. At the same time, modern methods of genetic correction can significantly improve the patient’s condition and reduce the risk of developing complications associated with pathology of the hematopoietic system.