Advanced muscle disease: symptoms, causes and treatment

The mitochondrial myopathy, under the protection of the subtitle muscle disorders, is a group of muscle neurological diseases caused by the damage to the mitochondria, which are small energy producing structures that act as cells for cells. Neurological cells in the brain and muscles require a large amount of energy, which is why it seems to be particularly damaged when a mitochondria counterbalance occurs, and some of the most common muscle disorders in the mitochondria include Kiris Sayer syndrome, symbolic epilepsy with torn red clothes, Encephalopathy with Mitochondria with browns, and strips -and -bak. Most cases of muscle disorder occur before the age of twenty in mitochondria, and often start by not tolerating exercises or muscle weakness during physical activity, the muscles can be tired or easily weakened. Muscle cramps are rare, but it can happen. Symptoms of advanced muscle diseases include symptoms of muscle diseases in mitochondria as follows: muscle weakness or intolerance of exercise. Heart failure or system disorders. Death. Movement disorders. Stroke -like episodes. Design. Blindness, eyelids and limited eye movement. Vomiting, nausea. Headache. shortness of breath. Causes and factors of the risk of broken muscle diseases in the following are an explanation of the most prominent causes and factors of the risk of infection with submitted muscle diseases: 1. The causes of infection with a submitted muscle can occur in the mobilized muscle diseases due to mutations in the body’s DNA, or by the DNA of the mutate. The former muscle disorders caused by DNA mutations can be inherited from one or both parents, or can be caused by spontaneous genetic mutations with the individual concerned. The forms of the submitted muscles caused by the mother’s mutations are often inherited, as women only pass the mitochondria -dna mutations through the egg, and men with mutations can be affected by the conditions, but it does not transfer to their children, and in some cases the mutations are spontaneous in the individual concerned. The forms of muscle diseases are often inherited in the mitochondria caused by deletion caused by spontaneous genetic deletion. 2. The risk of developing intramuscularly includes the risk of the disease with people with a family member with a genetic mut. The complications of the advanced muscle diseases include the most prominent complications as follows: The submitted muscle disorder can cause weakness and waste the muscles of the face and other neck, which can lead to problems with swallowing and in rare cases that impede the speech. People with imitating muscle diseases can suffer from poor muscles of the arms and legs. The disease sometimes affects additional tissue that is a great energy consumer, such as: the heart muscle and the central and oceanic nerves, where the heart infection leads to heart muscle disease. The infection of the nervous system is reflected in the occurrence of damage in the form of base arrogance or cerebral cortex, in addition to prejudice to the white matter, and it can also lead to a motor injury, mental or epilepsy. These disorders vary in intensity of gradual weakness to death. Diagnosis of advanced muscle diseases if he is suspected of submitting muscle diseases based on the physical symptoms of the patient, and its date is additional diagnostic tests, and these clinical diagnostic tests may include: including blood tests: including a full blood census and tests to search for high concentrations of lactic acid and other deformities. Urinet test: To search for abnormal levels of amino acids, glucose and other volatile levels. Discharge Monster Analysis: To search for high fat levels indicating a decrease in pancreas. Poor grain fluid analysis: to look for high protein levels. Imaging: MRI, computerized tomography, other brain imaging, muscle tissue or other organs. Electrical Planning: To discover the heart rhythm deviations. Echo diagram: to judge myocardial disease and other heart problems. Muscle biopsy: To look for rough red fibers that represent the reproduction of abnormal mitochondria. Biopsy: Draw a sample of the bone marrow and a microscopy. Genetic diagnosis test: Use blood, muscles, skin, saliva, hair follicles, urine deposits or other tissue samples to search for mutations. Treatment of advanced muscle diseases. There is no treatment for submitted muscle diseases, but treatment can help reduce symptoms or weakening of health as the treatment of patient to patient varies and depends on the specified disease that has been diagnosed and strengthened. However, there is no way to predict the patient’s response to treatment or prediction of how the disease affects this person in the long run, as two people will not respond in the same way in the same way, even if they have the same illness. Treatments may include the following: 1. Vitamins and nutritional supplements, including B vitamins, especially vitamin B1, vitamin B2 and alpha lipoic acid. 2. Exercise, including endurance and resistance exercises, where it is done to increase the size and strength of muscles, and include: tolerance exercises. Walking and running. Swim. Dance. Cycling. Weight lifting exercises. Arm strengthening exercises. Knee Extension Exercises. weightlifting. 3.. The maintenance of energy does not try to do much in a short time. 5. Avoid situations that may aggravate your medical condition and include the following: Exposure to cold or heat. Famine. Lack of sleep. Difficult situations. Use of alcohol and Room housing. 4. Other treatments may include speech therapy, physical therapy and respiratory treatment. Prevention of advanced muscle diseases cannot prevent the disease.