Creutzfeldt -jacob diseases, under the protection of Creutzfeldt -jacob diseases, is sponsored by Crotvild Jacob, one of the diseases that belong to the group of diseases that affect humans and animals, which are related to protein -like infectionism prions. This protein is important in all cells of the body, especially in the brain and the immune system, and it is found in two different cases so that it melts well in the water, and it can also be easily analyzed, so that its function leads to the brain to the full way. In the pathological cases, this protein melts only in fat as it cannot be analyzed and does not perform its function in the brain, and its accumulation in the body can cause an imbalance in the production of proper protein. Types of Crotozfeld Jacob disease There are many types of wild diseases (Priom). This kind of disease is called Coro, and it was common in the Papua New Guinea, is a habit of eating dead meat to immortalize his memory, which was very common. The second type was more common in animals, and it was known to the sheep herds of England for more than 200 years. Symptoms of Crotozeld Jacob disease collect poor protein through the brain and in the spinal cord they impede their work, and it causes many symptoms as follows: memory loss. Personal changes. insomnia. Trouble talking. Struggling to swallow. Speed cramps in the limbs. Causes and factors of the risk of Crotozeld Jacob disease produce crotozeld disease due to the accumulation of abnormal protein in the brain in large quantities, causing damage in many parts of the brain. Rotzfield disease factors There are many factors that increase the risk of crotozeld disease as follows: Age: Usually a possibility of disease in older life is increased. Genetic factors: This is by moving the genetic mutation of the injured father to the child. Exposure to the implant of polluted tissues: Some medical errors can cause the affected tissues to the patient, causing the disease. Complications of Crotozeld Jacob disease quickly develop Crotusvild’s disease, causing the appearance of many complications as follows: Loss of ability to deal with family and friends. Loss of self -care. Access in a long coma. Death. The diagnosis of Crotozeld Jacob disease depends on the diagnosis of this disease on the characteristic symptoms of the disease, and some other tests are performed as follows: genetic tests. ElectronceFalogram. Magnetic resonance imaging – MRI. These tests help to confirm the presence of bronch disease, but in order to reach the categorical diagnosis, the flawed protein must be identified and defined precisely, and the microscopic spongy form in the brain must be present. The treatment of crotus vild Jacob so far there is no effective treatment for this disease, and doctors usually focus on relieving pain and the symptoms of the patient. In fact, prevention of Crotozeld Jacob disease is no clear methods that help prevent the disease, but it is preferable to communicate with a consultant if a family member is infected with the disease.
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