Anemia that accompanies the imbalance of ethical erythrocytes

Anemia that accompanies the form of congenital red cells is an extensive name for a group of rare genetic diseases characterized for an unknown reason by a disorder in the production of red blood cells in the bone marrow. Manemia classification accompanied by the formation of congenital erythrocytes was arranged in 1967. This group of diseases up to three subgroups: 1. Aute anemia that accompanies the formation of the form of congenital erythrocytes is transmitted by the autosomal recessive heritage, and about 80 patients were diagnosed from different places from the world. Most patients of birth suffer from anemia and sometimes liver and spleen, and they also have symptoms of congestive cardicate cardiac – CCF. The degree of risk of illness during life change from simple anemia to attachment to blood transfusion. In patients with simple hepatitis, the liver and spleen can occur, and with aging hemochromatosis can arise, which requires treatment from some elderly people through iron bonding. A few patients suffer from a deviation in the bone building, especially the syndactic, and some patients respond to treatment with alpha interferon -alpha, but the mechanism is unknown. In electron microscope (electron microscope), stem cells can be seen, while the core building and the core membrane are not healthy. The variable gene in the disease has been identified on chromosome 15 and was recently distinguished, and the gene is encrypted in an unknown protein. 2. Acarmia that accompanies the form of the formation of erythrocyte, the most common form of this disease, which is also transmitted by recessive physical genetic genetics, this disease is characterized by anemia in different degrees of risk, but without attaching to blood transfusion. Inflammation of the liver can also appear, enlargement in the liver and in the spleen. During a later period, the disease of the precipitation of dye and gallbladder stones arises, and in the bone marrow it is possible to see double -nucleus cells. In the blood test, the red blood cells disintegrate into the patient’s body and go through the process of decomposing acid into the acid in a well -appropriate person in terms of blood type. By connecting an electric field to the red cell membranes, a quick movement can be seen in the cut. The gene is in chromosome no. 20 determined, but in about 10% of cases it is damaged by another dynamic that has not yet been determined. 3.. Anemia that accompanies the formation of erythrocyte grains, the third type, it is the very rare form of the disease and is transmitted with the prevailing physical genetic genetics. Most patients with this type of disease belong to one family from Sweden. Several cases of anemia that accompany the formation of congenital erythrocytes that do not suit one of the three groups above have been described, but it is not known whether they are typical images, but it belongs to the well -known groups, or is new groups. Causes and factors of the risk of anemia that accompanies the imbalance of ethical erythrocytes, anemia that accompanies the formation of congenital erythrocytes, is a genetic disorder caused by defects in the genetic code of the person, where scientists have discovered, related to anemia that is the form of congenital erythrocytes, but Perhaps what is the perhaps what the maybe of the maybe is what it might be what the might be of it, what might be what it might be of the maybe, what it might be that may be what the maybe, what might be what the might be, what it might be what the parts of the manner are the appearance of the disease. The diagnosis of anemia that accompanies the formation of ethical erythrocytes is similar to signs and symptoms of anemia due to the imperfect erythrocyte imbalance symptoms of other blood disorders, making the diagnosis difficult. This is unusual for patients with anemia due to a congenital erythrocyte imbalance of another condition, such as: hemolytic anemia, and the genetic evaluation gives them an accurate diagnosis. One of the most important tests the doctor requests is: blood tests. Bone marrow analysis. Investigations to find out the reasons for the incidence of jaundice. Some image and laboratory tests that measure iron concentration in the body. Genetic tests. Treatment of anemia that accompanies the form of congenital erythrocytes, depending on the severity of the disease and the symptoms that patients suffer from. Doctors treat patients with anemia who accompany the formation of ethical erythrocytes as follows: Blood transfusion: In the case of serious poverty in the blood volume in the body. Drug therapy: such as: medication that treats iron high in the blood (iron -caring drugs), and the alpha interferon -used specifically in the first type. Surgical operations: There are some serious cases that require the removal of spleen or gallbladder. Bone marrow transplant: Bone marrow transplant is the only treatment that causes healing of the disease, but it is not used in very severe cases. Doctors will determine the best approach to the treatment of the child’s condition based on a number of factors, including: age, overall health, disease intensity and interactions between medication or treatments. Due to the lack of a final treatment, except for the transplantation of the blood -forming stem cells, children and adolescents with anemia that accompany the form of congenital erythrocytes need long -term follow -up to monitor complications. The importance of following the problems of liver, endocrine and heart increases with the aging, due to the tension due to the low hemoglobin and the high iron level in the blood.