Can congenital muscular dystrophy be cured?

Congenital muscular dystrophy, if the condition is mild, can be **, daily muscular dystrophy, belongs to a kind of own genetic disease, serious is unable to **, active support** can maximize muscle function, delay or correct skeletal deformities, for bone deformities that have occurred, affecting limb function, can be corrected by surgery, symptomatic measures include mechanical ventilation, eye protection, seizure control, congenital muscular dystrophy, can be passed** Train and use nerve-relieving drugs to avoid further aggravation of symptoms, ** during the period, you must pay attention to keeping warm, avoid the body from getting cold, you can eat some high-protein, high-fiber and high-nutrient foods. Muscular dystrophy is mainly a muscle degenerative disease caused by genetic factors, and in addition to genetic factors, the patient's own genetic mutations can also cause the disease. Progressive muscle atrophy and weakness are the main clinical manifestations.

At present, although many scholars have explored the pathogenesis of muscular dystrophy, it is still unclear. The probable pathogenesis of pseudohypertrophy (DMD) is a defect in exon coding for the anti-dystrophin gene located in XPZI. The gene for faciculoscapulohumeral muscular dystrophy is mapped to 4935, and the gene for limb-girdle muscular dystrophy is mapped to chromosome 15 or 16.

There is a clear family history of the disease, in which males outnumber females, male:female: 1.

What should be done about congenital malnutrition in infants, first of all, it is necessary to go to the hospital to check the child's body, see what causes it, prescribe the right medicine, strengthen the child's care at ordinary times, pay special attention to the diet, eat more foods with high nutritional value, the child should also be well absorbed, and pay attention to the child's hygiene.

Congenital malnutrition in infants and young children is a relatively common symptom now, mainly because the food eaten can not be fully absorbed by the body, the body can not maintain normal metabolism, resulting in diseases, parents and friends of congenital malnutrition should pay more attention to it. Let's talk about what to do about congenital malnutrition in infants and young children.

Infant congenital malnutrition will cause a lot of nutrition to the physical and mental development of the baby, it will be stunted, and there will be emaciation, anemia, etc., so it is necessary to take a good **. If you find that the child has this problem, you must go to the hospital to check the child's physical condition to see what causes it, and then the next symptomatic **, you can use the method of medicine, but you must choose the right drug.

There is also the usual care and diet of children need to pay more attention, mainly in the diet to pay more attention, eat more nutritious value of food, food must be good digestion contains high energy, you can eat more protein, fat content of food, such as to give the baby the first thing is to drink milk, mainly drink some semi-skimmed milk, appropriate drink some soy milk, rice soup, fish mud soup these.

Infants and young children can still eat some milk, porridge, cakes, cakes and other food, to meet the needs of their own body, parents should not have the misconception that babies can not eat food, can only drink soup every day, eat more good food for children can improve their congenital malnutrition, but also to ensure the cleanliness and hygiene of food, as well as clean up the child's ** and oral hygiene, if necessary, but also to take care of their eyes.

What is said above is what should be done for congenital malnutrition in infants, because the child itself is relatively small, so parents and friends should pay more attention to it, if the malnutrition is really serious, it is best to go to the hospital for professional **.

Many people are born with congenital muscular dystrophy, which is very harmful to the patient, therefore, for congenital muscular dystrophy, it should be consolidated, so that the condition will recover faster, and the following experts will introduce it to you. 1. Patients with congenital muscular dystrophy should establish confidence, resolutely fight against the disease, and carry out some recreational activities appropriately, which can promote the patient to establish an optimistic and cheerful mood and establish the confidence to overcome the disease with strong perseverance. 2. Patients with congenital muscular dystrophy should do some physical exercise appropriately to help enhance their own immunity.

At the same time, self-massage to increase activity, promote blood circulation, and prevent muscle atrophy, but it should be moderate and not overworked. 3. Diet is helpful for congenital muscular dystrophy. Therefore, patients should eat light and nutritious diet, avoid or eat less greasy, thick-flavored, overheated, injured and fluid and damage to 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.

In addition, patients with congenital muscular dystrophy can also eat more vegetables and fruits such as cabbage, bean sprouts, tomatoes, hawthorn, mandarin oranges, and dates. While ensuring nutrition, weight should be properly controlled. 4. Congenital muscular dystrophy is a chronic disease, patients should keep the environment clean and quiet, pay attention to moisture and cold, and actively prevent complications such as respiratory tract infection.

Can children with congenital muscular dystrophy, muscle atrophy of hands and feet, muscle weakness, weakness up and down stairs, and muscular dystrophy be completely good?

Supplementary question: Many patients feel that muscular dystrophy is a disease that can be cured without medicine, and it is not curable, but it is not, muscular dystrophy is not a disease that is difficult to treat, but it is not incurable, these are two concepts, and the treatment of muscular dystrophy pays attention to ways and methods, and some doctors in some places have not heard of muscular dystrophy, in fact, this disease is not mysterious, but there are relatively few doctors who study this disease.

Additional question: Muscular dystrophy is mainly a muscle degenerative disease caused by genetic factors, and in addition to genetic factors, the patient's own genetic mutations can also lead to the occurrence of the disease. Progressive muscle atrophy and weakness are the main clinical manifestations.

A large proportion of patients are caused by genetic mutations. When the patient's family heard about the genetic cause, they were scared half to death, and the children went everywhere to check and test the genes. I was not at ease with the local examination, so I went to a famous hospital across the country for another examination.

As a result, I got a sentence "It can't be cured at all, this is a world problem, this is an immortal cancer". Every sentence pierced the heart, so that the patient's family was frightened and rushed to the doctor.

Additional question: Muscular dystrophy. Strong muscle marrow recovery soup is made of dozens of precious and pure Chinese medicinal materials such as saffron, centipede, eucommia, antelope antler, and ginseng.

From the inside and outside of the human body, it deeply regulates and dredges the meridians of the whole body, improves blood circulation, comprehensively regulates the five organs, strengthens the foundation and cultivates the yuan, restores sufficient qi and blood, stimulates yang qi, strengthens muscles and tendons, comprehensively improves the symptoms of neuromuscular diseases, and enhances the body's immune function. As a result, the human body's meridians are supplied with sufficient nutrients and accelerate metabolism, so as to open up meridian blockages, curb nerve atrophy and even relieve the disease. The active ingredients in it can repair the cranial neuropathy tissue, promote the repair and regeneration of neuromuscular cells, regulate the muscular nervous system in both directions, and fundamentally solve the disease.

No. "Congenital muscular dystrophy mainly includes early-onset and late-onset types, and generally can't**. Because of the presence of gene mutations in muscular dystrophy, it can lead to muscle weakness and atrophy, and some patients will have pseudogastrocnemius hypertrophy and connective tissue hyperplasia, which makes the muscles in a state of atrophy.

Under normal circumstances, only coenzyme Q10, ATP, vitamin E, etc. can be given to effectively improve the weakness symptoms caused by muscular dystrophy, improve muscle metabolic function, and delay the aggravation and development of the disease. ”

Congenital muscular dystrophy cannot be cured, such as Wilson's disease, methylmalonic aciduria combined with hyperhomocysteinemia, phenylketonuria, etc. At present, the disease is mainly symptomatic**, including nutritional support, respiratory support, reasonable care, long-term follow-up, etc. Some genetic or alternative treatments are still in the trial and have not been fully applied in clinical practice.

Congenital muscular dystrophy cannot be cured, such as Wilson's disease, methylmalonic aciduria combined with hyperhomocysteinemia, phenylketonuria, etc. At present, the disease is mainly symptomatic**, including nutritional support, respiratory support, reasonable care, long-term follow-up, etc. Some genetic ** or substitution** are still in the trial, and they have not been fully used in clinical practice.

Suffering from congenital muscular dystrophy, there is currently no good special medicine Bu Zhenwu, mainly through acquired physical exercise to improve symptoms. Proper physical exercise can promote muscle blood circulation, promote the development of the nervous system, and exercise the movement of joints. During this period, it can also be combined with acupuncture and massage or smoked with wormwood to promote blood circulation and improve muscle dystrophy.

It can also be administered intramuscularly with the energy brother and cons adenosine triphosphate with the help of drugs**.

No. Congenital muscular dystrophy is generally not curable. Congenital muscular dystrophy is an inherited muscle disease, which is characterized by skeletal muscle weakness and atrophy, and the onset is relatively insidious.

So far, there is no very good method, it is a difficult disease, and it can only be symptomatic and support Hehe**, increase the camp and normal activities. Orthopedics** is recommended to prevent and improve spinal deformities and joint contractures. ”

Muscular dystrophy is an inherited progressive muscle degenerative disease that is mainly manifested by progressive muscle atrophy and weakness, and muscular dystrophy is mainly a muscle degenerative disease caused by genetic factors.

Congenital and malnutrition is a problem that plagues the world, because there is no best way in medicine, patients generally need to do wheelchairs at the age of 20 or so, many scientists are currently studying congenital muscular dystrophy by injecting cells, but it is still in the experimental stage, basically no human experiments, if congenital muscular dystrophy occurs, it can only wait for scientific progress in the future to treat, and need to pay attention to nutrition at ordinary times.

Manifestations of congenital muscular dystrophy.

Benign muscular dystrophy, mainly X-linked recessive inheritance, is inherited through women, but male patients will develop the disease, generally speaking, at the age of 5 to 20 years will gradually onset, and then after 15 or 20 years can not walk, generally will not involve the myocardium, and will not appear intellectual disability, patients should exercise under the guidance of doctors at ordinary times.

The limbs generally appear pseudohypertrophy, children are likely to fall in early childhood, and the age of walking will be delayed, walking will also feel slow, and after falling can not get up, this is some manifestations of malnutrition, and will also show a duck-shaped gait, and the squatting position can only rely on two hands to support it, and then there is an Achilles tendon contracture, which needs to go to a tertiary regular hospital in time**.

Congenital muscular dystrophy is also relatively slow, generally symptoms appear around the age of 10, if the condition is mild, there may be no symptoms, the forearm muscles look very normal, and the patient's gastrocnemius muscle will become very large, but it does not affect the life of the person, muscle contractures may occur in the late stage, unable to move, and patients should not rush to the doctor, because there is no good way to do so.