Correct Disorders: Causes, Symptoms and Treatment

Challine disorders of glycosylation disorders with the disorders of congenital glycosel disorders are a genetic disease affecting all body systems, especially the nervous system. This disease was first announced in Belgium in 1980, and since then hundreds of cases have been announced around the world. Many proteins that produce the body need to make certain changes to perform their functions, and adding glycosille sugars is one of the most important of these changes. The process of adding sugars is actively related to a number of enzymes, and each enzyme has its own genes, and in the case of a mutation mutation, the enzyme does not serve its function and the process of association with glycosille stops. Symptoms of correction disorders with glycosilles differ in the risk of the disease with different types of disruption of glycosilles and the condition of patients, and the symptoms occur in many organs in the body. 1. Symptoms of general general glycosilles are: unusual facial and preventative features. Brain and nerve defects. Damage in heart function, digestive system, hormones, blood clotting, liver, kidneys, eyes and bones. 2.. Symptoms of glycosille disorders associated with age in each phase of life. The disease manifests with different symptoms and is suggested by the following: Symptoms of early childhood are one of the most important symptoms affecting the patient in childhood: the lack of growth. Mental disability. Heart problems, skin. The incidence of attacks (attacks). They are difficult. imbalance. Adult symptoms, but in adults, symptoms occur in the form of: a maturity. Eyes and bones problems. Causes and factors of the risk of glycosille disorders, in fact there are not many factors and causes that lead to the appearance of the disease. 1.. The cause of glycosilles. There are 11 types of correlation disorders. Each type is caused by mutations in different genes of the body. The surge is transmitted by a mechanism known as the autosomal recessive, in these kinds of genetics, each of the parents carries one mutation in its genes, while the second is without a mutation, that is, it is pregnant with the disease and is not sick and is not symptoms, and the child suffers from the disease only in the heritage of the mutation of the mutation. 2.. The risk factors increase the percentage of the disease in families consisting of religion that connect to family family members, that is, the marriage of family members, because part of their genes are shared, including genetic mutations, and in Europe the incidence of the disease reaches 1: 80.000 births. Complications of correction disorders with glycosille do not exist in reliable sources any installed risks and complications. The diagnosis of glycosille disorders is diagnosed with the following procedures: 1. The physical examination is diagnosed by the condition of the patient by seeing the characteristic signs of the disease on the patient’s body, and he is also asked about the symptoms he suffers from. 2.. A simple blood test is called transphericity isotyping, which is an iron carrier in the body, and it may also indicate some types of glycosel ingredient disorder. 3. The genetic investigation is a quick examination by which the mutations that cause glycosille deviation are known, and it helps to diagnose the disease early. Prepo -Diagnostic Diagnostic Mechanisms are currently available for a portion of people with glycosal disorders. As for the tests that measure the hypoglycaemia that causes the disease, it has not been used and has not been proven successfully. The treatment of glycosille disorders There is no cure for these diseases, and treatment is generally a supportive treatment to relieve the symptoms associated with the patient’s condition. The disease is treated as follows: Make sure you feed the patient: In the event that the patient is unable to eat food, a nutritional tube can be installed from the nose to the stomach. Career Therapy: By following physical therapy and teaching the child to express to prevent growth disorders. Epilepsy treatments: This is done using medication to treat epilepsy in case of attacks. Plasma transfer: To treat blood clotting. Surgical treatments for the eye: In the case of eye problems, surgical intervention requires. The treatment of hormone disorder: In some cases, disorders in the thyroid hormone can occur and are treated with medication. Give the patient albumin: Potassium can also be added to treat liver problems and prevent damage. Treatment by giving sugar: Some types of disorders may need sugar for patients for treatment. Prevention of Glycosil Association Disorders There are no ways to prevent this disorder as it can help reduce the marriage of family members who have genetic mutations that cause the disease to reduce the chances of its occurrence.