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Conduct physics**. **Physics of muscular dystrophy**, physics ** is to know a relatively good **, most diseases ** will generally use physics**.
Carry out the basics**. The basic ** is generally the use of drugs**, drugs ** is indispensable**, mainly based on traditional Chinese medicine prescriptions, with acupuncture and massage, which is also a common method for muscular dystrophy.
Conduct training**. Muscular dystrophy is mainly manifested by muscle weakness and contraction, so muscle training has a good effect, and you can use straightening, standing and moving or walking exercises for recovery exercises.
Perform TCM**. Muscular dystrophy is characterized by tiredness, weakness, and fatigue. The use of traditional Chinese medicine prescriptions to replenish qi and strengthen the spleen, activate the muscles and bones**, will also have a good effect on muscular dystrophy**.
Acupuncture and massage of acupuncture points can also be performed, which have a good effect on relieving symptoms.
Muscular dystrophy has a great impact on patients, and at present, we do not have many methods for muscular dystrophy, but as long as you follow the doctor's guidance, carry out targeted treatment against your actual disease, and maintain a good mood and mood, it is completely possible to achieve a very good effect.
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Muscular dystrophy has a poor prognosis in most cases and can eventually lead to disability and death. At present, there is no **method, mainly symptomatic and supportive**. Appropriate training, timely application of braces to support the child's limbs, as far as possible to maintain and prolong the child's ability to walk independently.
Low-dose corticosteroids can lower creatine phosphosaryosase levels but do not stop the progression of the disease. Gene substitution** and small molecule** methods such as antisense oligonucleotide-induced exon skipping are still experimental and are expected to improve disease outcomes in the future. Eat a balanced and nutritious diet.
Appropriate physical exercise to enhance resistance. For children with respiratory muscle involvement, respiratory tract infections should be avoided as much as possible, and respiratory tract management should be strengthened when respiratory tract infections occur.
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Disease analysis: The overall ** of muscular dystrophy is long-term persistent**, and it also takes more than 1 year after the symptoms are controlled. Generally, symptomatic support is the mainstay, drugs are mainly vitamin E, inosinate, nicosamide, and others**training are the mainstay.
1. Drugs**.
1. Vitamin E: It is one of the commonly used antioxidants, and the main purpose of its application is to alleviate the symptoms of muscle atrophy and promote the control of the disease.
2. Inosine: It can improve the body's protein and ATP levels, thereby relieving muscle weakness and atrophy, and is an important adjuvant drug for this disease.
3. Lingspor polysaccharide injection: the main effect is atrophic muscle rigidity and progressive muscular dystrophy, as well as related immune dysfunction and other symptoms, which can effectively control the disease process.
4. Nicosamid: It is a commonly used respiratory stimulant, which can control the symptoms in time during the acute attack of respiratory failure and avoid life-threatening.
2. Surgery**.
Complications such as joint contractures and spinal deformities caused by muscular dystrophy and complications such as cataracts can be surgically performed**.
3. Others**.
Progressive muscle weakness and muscle atrophy can lead to a significant decrease in the patient's mobility, and timely training can alleviate muscle weakness and slow down the course of the disease.
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Physical** and massage can improve local blood circulation and prevent joint contractures in children with muscular dystrophy. Surgery**DMD can be considered for Achilles tendon release and scoliosis orthopedics in the early stages of DMD to try to prolong the duration of limb movement.
Basic substitution**This is currently recognized as the most promising method to improve the function of muscle fibers to produce dystrophin in children. In addition, stem cells are progenitor cells that can differentiate into a variety of tissue cells, which have been shown to partially repair damaged muscle tissue, providing new prospects for DMD**.
The diagnosis of muscular dystrophy is not difficult to diagnose based on the specific distribution and typical signs of insidious onset, muscular atrophy of the affected skeletal muscles, and weakness. Measurement of serum enzyme activity, electromyography, and muscle biopsy can provide evidence for diagnosis and differential diagnosis. Some types of muscular dystrophy still need to be differentiated from polymyositis, motor neuron disease, or myasthenia gravis .
The diagnosis of DMD and BMD is based on the detection of dystrophin deficiency or abnormality in the biopsy muscle and the detection of the dvstronhin gene variant on peripheral blood leukocyte DNA analysis.
In view of the progressive aggravation of muscular dystrophy and the high rate of disability, it is necessary to pay attention to early development and improve the quality of life, especially if there is a similar history in the family, it is necessary to pay attention to it and check and diagnose it as soon as possible.
**During the period, avoid smoking and alcohol, avoid spicy and salty food, avoid wind and cold, prevent cold, drink more water, eat more food containing calcium and zinc, keep a good mood, exercise appropriately, the patient's family should cooperate with the massage, and the patient himself should overcome difficulties and insist on proper exercise.
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Muscular dystrophy can be delayed by medications, and orthodontic surgery can be performed in patients with lumbar spine, muscle, or bone and joint atrophy. In addition, the patient's mental health should be paid attention to, and if necessary, the patient's psychological counseling should be carried out**.
When it comes to muscular dystrophy, many people will inevitably feel unfamiliar, which is a genetic and inherited disease, usually manifested by mobility disorders, which has a great impact on and damage to the lives of patients. There are many methods of muscular dystrophy, generally including drugs, traditional Chinese medicine, surgery, etc., and when it is found that the patient has psychological problems, it should also be psychologically treated in time. Let's take a look at the details.
1. Drugs**.
There is no drug for muscular dystrophy, but other drugs can be used to relieve muscle spasms, such as epilepsy medications, immune preparations, etc. In addition, it can also be combined with some suitable nutritional drugs to protect nerve and muscle tissue, and drugs such as vitamin E and glucose are recommended. The specific drug needs should be selected under the guidance of a specialist as much as possible.
2. Traditional Chinese Medicine**.
When muscular dystrophy develops to a certain extent, it will cause damage to the function of the patient's heart, spleen, stomach, intestinal tissues and other organs, which can be regulated by traditional Chinese medicine, specific measures generally include acupuncture, moxibustion, traditional Chinese medicine, etc., but the conditioning cycle may be relatively long, and patients should remain patient.
3. Surgery**.
The main symptom of muscular dystrophy is the atrophy of muscles, bones and joints, and orthodontic surgery is required if necessary to ensure the quality of life of the patient**. After surgery, attention should be paid to the improvement of diet and nutrition to promote physical recovery and prevent the occurrence of postoperative infection.
4. Psychological intervention.
Affected by the disease itself, patients with muscular dystrophy are prone to problems such as low self-esteem and anxiety, which requires timely psychological intervention to guide patients on the basis of symptomatic treatment. Family members should also actively encourage the patient to communicate and interact with others, and help the patient to go out and play appropriately.
In addition to the clinical aspects, it is also necessary to actively carry out appropriate exercises in life, and you can develop an exercise method suitable for the patient under the guidance of a specialist. In addition, patients with muscular dystrophy should also pay attention to dietary supplementation, especially protein foods should be eaten more, but attention should be paid to maintaining weight, and high-fat foods should not be consumed too much.
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I know a person who has been suffering from muscular dystrophy due to her parents' genetics, and she has been a key target of all of us since she was a child, and her relatives have been keeping an eye on her every move, and have taken her to see many doctors, and she has taken care of her every day. Because most patients with muscular dystrophy have poor physical fitness, it is also essential to achieve a reasonable combination of meat and vegetables in their diet, enhance their physical fitness, and keep warm. Although people with muscular dystrophy have little energy, moderate exercise is necessary.
Step Method:
1. Patients suffering from muscular dystrophy generally have a much lower physique than the original, and their immunity and resistance are insufficient, so it is necessary to actively prevent various diseases, pay attention to heat preservation, moisture and cold, so as to avoid colds, respiratory infections and other complications.
2. Insist on exercising, in ordinary times, we should do more physical exercise, self-massage, to promote blood circulation, to avoid the symptoms of muscle atrophy, but should be moderate, not overworked. This is the most effective way to prevent muscular dystrophy.
3. Patients with muscular dystrophy need a quiet environment, should ensure a quiet environment, do a good job of moisture and cold prevention measures, and actively prevent respiratory tract infections, which can effectively prevent the occurrence of muscular dystrophy. If you want to recover as soon as possible, proper exercise is indispensable.
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1. Appropriate exercise, self-massage to increase activity, promote blood circulation, and prevent muscular dystrophy, but it should be moderate and not overworked. 2. The diet should be light and nutritious, avoid eating or eating less greasy and thick overheat, injuring fluid and damaging the spleen and stomach, and eat more fish, eggs, chicken, lean pork, etc., but not too much, so as not to damage the spleen and stomach. Vegetables and fruits such as cabbage, bean sprouts, tomatoes, hawthorns, mandarin oranges, and dates can be eaten more than cherry.
While ensuring nutrition, weight should be properly controlled. 3. Keep the environment clean and quiet, pay attention to moisture and cold, and actively prevent complications such as respiratory tract infections. 4. Maintain a happy mood, adhere to appropriate recreational activities, promote patients to establish an optimistic and cheerful mood, and establish the confidence to overcome the disease with strong perseverance.
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To date, there is no specific approach to progressive muscular dystrophy, but symptomatic and supportive measures such as increased nutrition, normal activities, physical and orthopedic methods can prevent and improve spinal deformities and joint contractures, which are important for maintaining motor function. Because it is a lesion of the muscle itself, especially for patients who progress faster than oranges, they are not encouraged to do more strenuous exercises, so as not to aggravate the condition. Drugs such as coenzyme Q10, ATP, vitamin E and other drugs can be selected, because there is no effective method at present, so it is particularly important to detect the carrier Wu Hong, carry out prenatal diagnosis, and induce abortion of the diseased fetus.
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There is currently no specific method for this disease. Only symptomatic and general support, appropriate functional exercises, full passive movement of each joint, acupuncture, massage, etc. can delay the occurrence of more serious muscle weakness, muscle atrophy and joint contracture. Active prevention and prolongation of respiratory infection are valuable for prolonging the survival of patients.
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Many people will have physical malformations, or some babies will have deformities after birth, or just some people who have heard that they will get polio. There are reasons for this, because most of the diseases in your body are also caused by some malnutrition. Many people are malnourished.
But this situation is generally muscular dystrophy, so how about muscular dystrophy?
How to muscular dystrophy**.
First of all, it is necessary to check the basic physical condition of the patient and find the root cause of the disease, muscular dystrophy is mostly caused by visceral problems such as liver and kidney deficiency or spleen and stomach disharmony. Use traditional Chinese medicine and instruments to dredge the meridians.
Regulates the qi and blood of the whole body, so that after the growth factors reach the lesion, they can repair damaged and necrotic muscle cells, remove the inhibitory molecules that inhibit muscle cells, and regulate the structural and functional protein gene expression of target cells, so as to repair the necrosis of muscle cells caused by gene defects, replenish muscle fibers, and make muscle cells no longer necrosis.
What causes muscular dystrophy.
Myotonic myopathies are a hereditary disorder. Myotonic dystrophy is inherited in an autosomal dominant manner. Congenital myotonia is also inherited in an autosomal dominant manner. Congenital paramyotonic disease is caused by an autosomal mutation, and diet can regulate myotonic myopathy.
Diet and myotonic myopathy of the onset of the disease, the development of the disease, ** are related, as mentioned earlier, the onset of ankylosing spondylitis is related to intestinal infection, overeating, unclean diet will increase the chance of intestinal disease, so the diet should be regular, and pay attention to hygiene, to prevent intestinal infection.
The symptoms of muscular dystrophy are as follows:
First, when young children suffer from muscular dystrophy, the main symptom is that they walk slowly, and the walking age is delayed, and they are prone to falling, and it is difficult for them to get up after falling. >>>More
Muscular dystrophy is a group of diseases with progressive muscle weakness and muscle wasting due to genetic mutations that are passed down from blood to offspring. Genus. >>>More
Congenital ones are generally born when they are young, and they generally do not live to be twenty years old. The quality of life is not mentioned. It can't be cured at the moment. >>>More
In the later stage, it will seriously endanger life in time**.
1. Facicoscapulohumeral muscular dystrophy.
If the patient belongs to facicoscapulohumeral muscular dystrophy, it will generally occur in adolescence, after the onset of the patient's upper eyelids begin to droop, the frontal lines and nasolabial folds become more and more shallow, the upper limbs can not be raised or need special force to lift, and the patient is particularly difficult to do frowning, closing eyes, closing mouth, cheeks and other movements, biceps, deltoid and other muscles will have obvious atrophy symptoms. >>>More