Myasthenic dystrophy Is muscular dystrophy muscle weakness?

The disease should be symptomatic and general support, under the guidance of the doctor, the application of inosine, galantamine, vitamin E, adenosine triphosphate, nandrolone phenylpropionate and other drugs, if necessary, can be used traditional Chinese medicine, can achieve a good **remission, alleviate the child's condition, during the period of taking the drug, should also cooperate with appropriate functional exercises, pay attention to the full passive movement of each joint, can play a very good auxiliary ** effect, is conducive to the child's physical recovery, This reduces the harmfulness of progressive muscular dystrophy.

In addition, massage, acupuncture, massage and other methods can effectively delay more severe muscle weakness and muscle atrophy, which brings more help to the recovery of muscle health of children. In addition, it is necessary to actively prevent respiratory infections early, especially for patients with prolonged disease, which brings high value. If the child's condition is severe, corticosteroids can be used for DMD**, which can effectively improve the child's muscle strength and motor function, and achieve the effect of delaying the progression of the disease.

This condition is usually caused by a normal heart disease. It is recommended to go to the hospital for a check-up, and it is also recommended to take a chest X-ray examination to avoid being caused by other diseases, and to usually supplement more vitamins.

Beijing Deshengmen Hospital of Traditional Chinese Medicine-Yin Shirong-Department of Impotence-Chief Physician-What are the types of muscular dystrophy?

Muscular dystrophy is caused by a genetic abnormality, while muscle weakness is not caused by a genetic abnormality. Muscular dystrophy is a symptom of muscle atrophy and weakness, and muscle weakness is a symptom of weakness of the whole body or part of the skeletal muscles, and the body is prone to fatigue.

The poor muscular vegetative chain is a genetic abnormality, and the common symptoms of the disease are skeletal muscle atrophy and weakness; It is still unclear what mechanism genetic factors cause muscle degeneration. In the advanced stages of the disease, the patient may also be completely immobile, accompanied by symptoms such as contractures of the limbs. Some patients will have symptoms such as lung infections and pressure ulcers, which may lead to the end of life at the age of 20.

More than half of patients suffer from heart damage and a corresponding decline in intelligence. Some patients with muscular dystrophy may have impaired motor function or even paralysis; For muscular dystrophy, there is currently no effective drug for treatment.

Myasthenia is relative to muscular dystrophy, and it is possible that some muscles will recover after rest and medication**; However, it is also possible that the condition may worsen after remission**. The disease is divided into ocular muscle types, i.e., levator palpebrae or ocular weakness, bulbar muscle involvement, and generalized. Depending on the results of the test, the symptoms of muscle weakness can be relieved by plasma exchange or medication**.

Anticholinesterase drugs are one of the most common** drugs for muscle weakness and are effective in relieving or restoring some symptoms.

Muscular dystrophy and XinXun muscle weakness are not exactly the same concept, but there is a correlation between them. Let me explain it for you:

Muscle atrophy is a decrease in the volume and mass of muscle tissue, resulting in a decrease in muscle size and strength. This can be caused by not using certain muscles for a long time, age, lack of exercise, disease, or other factors. Muscular dystrophy not only affects the strength of the muscles, but can also affect the body's function and daily activities.

Muscle weakness is a decrease in muscle strength, making it more difficult to perform daily activities. Myasthenia can be a consequence of muscular dystrophy, but it can also be caused by other factors such as nerve problems, diseases, medications***, etc.

Although there is an association between muscular dystrophy and muscle weakness, they are not equivalent. Muscular dystrophy can cause muscle weakness, but muscle weakness does not necessarily mean muscular dystrophy. If you are experiencing muscle weakness or are concerned about muscle health issues, it is recommended to consult a doctor for professional evaluation and guidance.

Based on your symptoms, physical exam, and possible test results, your doctor can determine the cause of the problem and develop a corresponding ** or intervention plan.

It will make the body lose strength.

Muscular dystrophy is a type of muscle disease caused by genetic defects, mostly seen in young children, with muscle weakness and muscle atrophy as the main manifestations, muscular dystrophy is generally accompanied by slow walking, calf muscle hypertrophy, mental retardation, retinal damage and skeletal muscle atrophy. Muscular dystrophy mostly occurs in early childhood, and is manifested by delayed walking age, inability to maintain balance, symmetrical weakness and atrophy of limb muscles, slow walking, difficulty in getting up and down, difficulty and effort in going up and down stairs, inability to touch the ground with heels, and cold, hard, and coarse calf muscles. In addition, there is facicoscapulohumeral muscular dystrophy, which is mostly manifested as not closing the eyes tightly during sleep, weak blowing, and a wry smile, and the first symptom of limb-girdle muscular dystrophy is weakness and atrophy of the pelvic girdle muscles, and muscular dystrophy can also lead to eye problems, mostly manifested as ptosis and chronic progressive extraocular muscle paralysis.

What complications can muscle weakness cause? Muscle weakness, like many diseases, can lead to many complications once it is developed. Complications of muscle weakness will increase the difficulty of myasthenia in the process.

In this regard, we must pay attention to the complications of muscle weakness, so, what complications can muscle weakness cause? Myasthenia falls under the category of "impotence syndrome" in traditional Chinese medicine. It is a relatively complex disease, and at the same time, neurology experts pointed out that patients with muscle weakness should pay attention to the occurrence of other diseases, so what diseases will occur?

Here's a closer look.

Intermediate progressive spinal muscular atrophy": the age of onset is within the years, the disease progresses relatively slowly, the general muscle weakness symptoms of the lower limbs are heavier than the upper limbs, the trunk muscles are not very serious, the head can be erected, can sit, but can not walk and stand, can live to adolescence, and even live to adulthood, but spinal deformation can occur. "Juvenile spinal muscular atrophy":

The disease generally occurs after the age of age, up to 0 years old at the latest, the disease progresses slowly, and the disease can no longer worsen after the age of 3-4 years, some muscle weakness is very mild, can stand and walk, and there are also progressive exacerbations.

It should be distinguished from congenital muscle weakness, progressive muscular dystrophy, and progressive neuropathic muscular atrophy. Congenital myasthenia is more common in newborn infants, and the muscle weakness is non-progressive and gradually improves. The age of onset of progressive muscular dystrophy is mostly around 5-6 years old, the onset is slow, the lower limbs are weak, the gait is swaying, the gastrocnemius muscle is more likely to be pseudohypertrophied, the electromyography shows that the myogenic damage CPK and GAT are more elevated, and the progressive neuropathic muscular atrophy also occurs after the age of 6, the lesion is located under the knee, the feet cannot be dorsially flexed, and the downward is overhanging.

The complications of myasthenia have been described above, and it is hoped that patients will be brought to their attention and that early intervention will be carried out for myasthenia**. Kong Biaoru, an expert from Changchun Lantian Hospital, said: Traditional Chinese medicine conditioning is the most beneficial method for patients with muscle weakness.

After the phase III clinical trial and the actual effect feedback of the patients, it was shown that when the total effective rate of the decoction was reached, the general patient took 1 course of treatment, the condition was significantly controlled and improved, and the effect of the early patient was more obvious, and the patient could be cured after 4 courses, and the patient was not followed up after recovery.

Patients with muscular dystrophy may have the following symptoms: first, the symptoms of fatigue, which may not have any predisposing factors at the time of initial consultation, and fatigue may be cyclical, that is, muscle weakness will occur at a specific time every day, and with the aggravation of fatigue, even unable to walk upright; Second, in the case of muscle atrophy, you can eat and drink normally, but the muscles will have progressive atrophy and slender limbs; Third, muscle tone is significantly reduced, muscle tone refers to the tension maintained by the muscles when they are inactive, if the patient's joints are passively stretched, the muscles will reflexively produce tension, so as to maintain the stability of the joints and prevent the joints or overactivity. Patients with such diseases may feel a decrease in muscle tone and weakness all around their joints when they stretch their joints.

Muscular dystrophy is a group of inherited muscle degenerative diseases, mainly caused by genetic abnormalities, and patients often have genetic defects and are familial clusters. Some patients have no history of the disease and are caused by genetic mutations.

1. Genetic defects.

Genetic defects can lead to abnormalities in the proteins that maintain the structural and functional stability of skeletal muscle cells, affecting the normal movement of associated muscles. For example, patients with DMD or BMD malnutrition are affected by decreased dystrophin synthesis. Dystrophin acts as a scaffold to protect muscle cells from damage by protecting the muscle membranes from the forces generated by contraction.

2. Family clustering.

Muscular dystrophy can run in multiple families or cause it first.

3. Gene mutations.

Some patients do not have a family history of muscular dystrophy and may have a new genetic mutation. This is rare.

Muscular dystrophy is a genetic disorder.

Muscular dystrophy is a broad concept. Ordinary people will atrophy their muscles.

It is understood to be muscular dystrophy, but muscular dystrophy refers specifically to muscles or muscle fibers.

Membranes, mainly changes in myofiber membrane proteins, and sometimes changes in the skeleton proteins in muscle fibers, resulting in muscle cells unable to maintain normal physiological functions, and gradually die, lose and cause muscle atrophy and weakness. In general, there are many types of muscular dystrophy, which are as follows:

1. The most common is called progressive muscular repentance.

Refers to a group of the most common fatal and disabling diseases caused by dystrophin gene mutations, usually in boys, at the age of 3-4 and 4-5 years, and in the age of 10 years, they will lose their ability to exercise and be paralyzed in bed;

2. Limb-girdle muscular dystrophy, myotonic muscular dystrophy, face-shoulder-humeral shirt rental muscular dystrophy, oculopharyngeal muscular dystrophy, congenital muscular dystrophy, etc. can be covered in muscular dystrophy.

Muscular dystrophy, also known as progressive muscular dystrophy, is a hereditary muscle disease, chronic progressive exacerbation is mainly manifested by muscle weakness and muscle atrophy, which can be roughly divided into several types, the most common is pseudohypertrophic muscular dystrophy, including two types: 1. Duchai refers to ul-Hing's muscular dystrophy; 2. Baker muscular dystrophy. Amic muscular dystrophy also includes myotonic dystrophy, limb-girdle muscular dystrophy, facicoscapulohumeral muscular dystrophy and oculopharyngeal muscular dystrophy, etc., each type of manifestation and inheritance is different, but there are muscle weakness and atrophy, sometimes accompanied by cardiac abnormalities.

At present, muscular dystrophy lacks specific and effective **, and it is still mainly exercise-based, and drugs that can be appropriately supplemented with nutrition, such as creatine or hormones, immunosuppressants and other drugs.

In general, electromyography shows myocthenic injury pulverization, proximal atrophy and fissure, and some patients have fat hyperplasia in the calf or shoulder, muscle hypertrophy and weakness. Depending on the degree of involvement, most patients present with proximal weakness and atrophy, duck gait, weakness, easy falls, bedridden, respiratory failure, and premature death. Choosing Healing Formula can help patients prolong their lives and control their condition.

Believe that you will recover to a better degree.

Muscle wasting is a disease or symptom that refers to a group of syndromes in which the body or local muscle tissue forms a metabolic disorder state in which the muscle supports the breakdown of proteins due to insufficient nutrient intake or metabolic disorders, resulting in the decline and quality of muscle tissue. Muscular dystrophy is a complex physiological state, according to statistics, about 34% of patients, especially the elderly and patients with chronic diseases, will be in a state of muscular dystrophy for a long time.

Muscular dystrophy.

There can be many causes of muscular dystrophy, but common ones include:

1.Malnutrition: Long-term intake of nutrients or malabsorption, such as anemia, gastrointestinal diseases, etc.

2.Long-term bed rest: long-term bed rest and lack of exercise, resulting in muscle atrophy and hand contraction.

3.Diseases: Certain chronic diseases and infections such as cancer, liver or kidney disease, connective tissue diseases, fractures, injuries, etc.

4.Medications***: Certain medications, such as hormones, antibiotics and chemotherapy drugs, can have a negative effect on muscles.

5.Excessive exercise for a long time: Excessive exercise, training, etc. lead to an imbalance in the metabolism of the body, and muscle atrophy will also occur.

Common symptoms of muscular dystrophy include weight loss, muscle weakness, muscle atrophy, decreased range of motion, fatigue, and weakness. For people with muscular dystrophy, it is extremely important to choose the right method for them. Proper diet, increased exercise, and rational use of medications are all possible methods, but they need to be done under the guidance of a doctor.