Miers anemia: The method of conducting the investigation and analyzing the results

Fanconi’s anemia testing under the protection of the anesthetic anemia is diagnosed by the DNA (DNA), which is the genetic substance of the body to detect the gene that causes this disease. When we talk about this serious genetic disease, which is a shortage of red blood cells and later leads to a shortage of other blood cells. The disease is also the appearance of several changes in the skeleton, especially in the fingers. Cancer, especially leukemia, appears at an early age in a large part of those with this disease. There is a possibility for a child with a disease only when the parents carry the gene that causes the disease, and this may be known by performing the oxygen -oxygen core acid examination for genetic diagnosis before wearing a woman and is performed by taking a blood sample. When is the examination performed? Anecdotal anemia examination can be performed in couples, both of which are of one ethnic origin. In these population groups, there is a high percentage of this gene, due to the presence of a special mutation for them, as it is genetically diagnosed before pregnancy. Another reason for performing this investigation is for diagnosis before pregnancy in families that are transmitted with heredity in this disease. In addition, there is another type of investigation into the genetic substance that can be performed for children who are suspected of the disease, depending on certain pathological signs, such as having an unknown anemia or another problem in blood cells, such as examining chromosomes. Preparation for the exam is no special preparations before the exam. The risk category with people with infectious diseases transmitted by blood such as hepatitis (HIV, hepatitis) and others, the doctor suggests it. Infectious diseases do not form a contraindication for a diagnostic diagnosis of anesthetic anemia, but medical staff should be careful to prevent the transmission of infection to them. Related diseases include related diseases of the fanconi anemia. How to perform the examination is conducted by the DNA examination in a way similar to the way the fragile X syndrome, FXS is performed by taking a blood sample, as the person subjected to the investigation protrudes his hand on a flat surface or a table vessail and then the top of his arm is tied with a rubber band. A person is expected to hold his hand, which helps to find a good blood vessel to take a blood sample from him, often in the elbow or forearm. The sample is sometimes taken from the back of the palm of the hand. If you find a suitable vein, the area is sterilized with alcohol, and then tingle the vein with a delicate needle tied with a test tube, with a stock or a butterfly tool used to extract the blood. The person may feel the light pain caused by the needle tingling. Later, the examiner drew the required amount of blood into a special laboratory tube. After completing the withdrawal of the blood, the needle is quickly removed from the vein, and then the pricklass is immediately pressed by a handkerchief to prevent bloody bleeding in the tingling area. The exam takes almost five minutes. The test tube is transferred to a special laboratory to investigate the genetic material in the blood cells. After the investigation, you can stop pushing after 2 – 3 minutes or when the local bleeding stops. Light local bleeding often occurs in the tingling area, but it disappears within a few days and does not need treatment. In rare cases, acute, painful and swollen hemorrhagic bleeding can occur in the tingling area, which requests to inform the doctor to exclude infection in the intravenous area of ​​venous inflammation that requires treatment. General warnings There are a very little risk of performing the genetic material by taking the blood sample and contains a sense of minor pain or bruises at the place where the needle is fitted, but most of these symptoms usually disappear quickly. During pregnancy: There are no special warnings. Breastfeeding: There are no special warnings. Children and babies have no special warnings. Elderly: There are no special warnings. Management: There are no special warnings. Medicines affecting the result of the investigation are no special warnings. The analysis of the results today is known to be the specified place for a group of genes that cause the disease, and the genetic mutations can be distinguished in an easy and effective way if present. 13 of the genes that cause this disease have been discovered, including: Fanca, Fancb, FANCC, Fancd1, Fancd2. The results of the Anting blood poverty clearly examine and detailed whether there is a mutation in one of the genes that cause the disease, and according to the type of mutation, the risk of the birth of a sick child or a pregnant woman is determined.