Immunological Deficiency Primary

Primary immunological deficiency (I.N.P.) is a condition in which the body is unable to effectively fight infections and other diseases caused by viruses, bacteria or other microorganisms. This may be caused by genetic defects, immune system development disorders, or other factors.

I.N.P. is a fairly common disease that can occur at any age. Symptoms of I.N.P. may be different and depend on the type of disease. Some of these may include frequent colds, skin infections, skin ulcers, digestive problems and other illnesses.

Treatment of I.N.P. usually involves the use of immune-stimulating drugs such as interferon and antigens, as well as other treatments such as diet and lifestyle changes. In some cases, a bone marrow or other organ transplant may be needed to restore the immune system.

It is important to understand that I.N.P. can be a serious condition that requires ongoing treatment and monitoring. Therefore, if you have any symptoms associated with I.N.P., it is necessary to see a doctor for diagnosis and treatment.

Immunological deficiency (ID) is a disease in which the cells of the immune system do not fully perform their functions, and the body is unable to protect itself from pathogenic agents. One of the varieties of Indus is primary Indus, which develops even before birth against the background of mutations of genes responsible for the development of lymphoid tissues, as well as under the influence of negative factors acting on the mother’s body.

If we look at the process of the immune response that occurs during infections of any etiology, we will see behind it a complex chain of reactions of interaction between antigen proteins and anti-human antibodies. During any inflammation in the body, the process of producing antibodies to its own tissues and cells occurs, often ending in negative consequences. However