Edinosin de Amalese: symptoms, causes and treatment

Adenosingaminase deficit under the protection of adenosing aminase is a main function in the process of destroying and rebuilding the core as it is responsible for converting one of the above building materials called adenosine to another average stage called einosin. Essin can decompose, so that it is secreted by urine in the form of urica acid, or it can be used to rebuild new nucleic acids, this enzyme is found in all cells of the body, but if shortened in the body, the most damaged cells of this deficit are the lymphocytes. The lack of lymphocytes that make up the main arm of the cellular immune system is the cause of the acute immune deficit that distinguishes this disease, as the gene responsible for the adenosine de Amins on chromosome no. 20, and in the case of a specific disease responsible for the injury of 15% of all patients suffering from an acute deficit of primary immunity in satisfaction and children. Symptoms of adinosen denisiendinams are the most important symptoms of adenosin de Amalez in the following: pneumonia. Chronic diarrhea. The scattered rash. Capable children also grow in much slower than healthy children, and some suffer from growth. The causes and factors of the risk of lack of adenosine de Amalez provide a lack of adenosine de amalez due to the presence of mutations in the gene (ADA), as this gene is responsible for the production of the enzyme, this enzyme is found more active in specialized white blood cells called lymphocytes. These cells protect the body from potentially harmful bodies, such as: bacteria and viruses by making immune proteins called antibodies or by directly attacking the affected cells. Complications of the lack of adenosine de Amalez In the development of an adenosine de Amalez enzyme, it leads to a lack of immune cells, leading to a weak immune system and thus the body becomes vulnerable to different diseases and infections, causing the following: the upper respiratory infections. Regular ear infections. Chronic damage to the lung may have patients over time. Malnutrition and other health problems. Diagnosis of the deficiency of adenosine de Amalez The disease is diagnosed based on appropriate laboratory tests, and as we mentioned above, the low number of lymphocytes is in the bloodstream, ie less than 500 cells per cubic millimeters, and almost a complete lymphocytes shortage. The final diagnosis is determined by measuring the ratio of the enzyme within the red or white blood cells. Most individuals suffering from Adenosin de Amins are diagnosed in the first six months of life, and without treatment these children do not live after the age of two. In about 10% – 15% of cases, the rise of immune deficiency is delayed between 6-24 months or even the age of adulthood, as immune deficiency in these late cases is less severe. Treatment of an adenosine de Amalez is the best treatment for this disease, is the skeleton of the bone marrow, as the process of inserting the bone marrow cells to switch the affected cells to the patient, that is, which cannot secrete the missing enzyme as new cells produce the enzyme and reduce the percentage of toxic substances in the body. The success rate of marrow transplants rises when the appropriate percentage between the donor and the recipient is more, so it is preferable to receive donation from the brother or sister; Because they have the same tissue classification. Recently, however, successes have proclaimed goodness in this area. The principle on which this method depends, the extraction of damaged cells from the body of the patient and the laboratory was restored by entering a healthy gene, and then injected it into the patient’s body. There are some technological, material and ethical problems that have not yet been solved, which prevent the conversion of this treatment for known and routine treatment. The prevention of a lack of adenosin de Amins cannot prevent the disease.