Is muscular dystrophy caused by facial muscle involvement?

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.

Patients with muscular dystrophy may show the following symptoms: 1. Symptoms of fatigue, which may be caused by fatigue without any precipitating factors at the time of initial consultation, and fatigue may be cyclical, that is, muscle weakness will occur at a specific time every day. As fatigue worsens, it is not even possible to walk upright.

2. In the case of muscle atrophy, you can do normal activities and diet, while the muscles will have progressive atrophy and slender limbs. 3. Muscle tone is significantly reduced, and muscle tone refers to the tension maintained by muscles when they are inactive. If the patient's joint is passively stretched, the muscles will reflexively produce tension, which in turn will maintain the stability of the joint and prevent the joint from overmoving.

Patients with this type of disease may feel a decrease in muscle tone and weakness all over their joints when they stretch their joints.

The main symptoms of muscular dystrophy are slowly progressive, symmetrical muscle weakness and atrophy without sensory deficits. According to the type of disease, there are different characteristics in clinical manifestations.

Diseases with progressive muscle weakness and muscle atrophy as the main symptoms caused by genetic mutations, Peitu Ziyuan Tang Chinese medicine is taken orally**.

Congenital abdominal wall muscle dysplasia, inflammatory myopathy, progressive muscular dystrophy, periodic paralysis, myotonic dystrophy, mitochondrial myopathy, etc.

Muscular dystrophy is a muscle degenerative disease caused by genetic factors, and in addition to genetic factors, mutations in one's own genes can also cause the disease. Progressive muscle weakness and atrophy are the main clinical manifestations. Depending on the type of muscular dystrophy, the rate of progression varies and the severity of the disease varies.

Muscular dystrophy is divided into many types, generally divided into benign and malignant, among them, benign muscular dystrophy is relatively optimistic in terms of **, because the onset time is late, the progression rate is slow, and there is a normal life expectancy. Therefore, benign muscular dystrophy is relatively improved and the prognosis is better. In addition, malignant muscular dystrophy has an early onset and rapid progression, and children begin to have weakness in walking, difficulty in squatting, and difficulty in going up and down stairs after walking**, which has a great impact on life expectancy.

Muscular dystrophy is a disease that causes progressive muscle weakness and atrophy due to genetic defects.

Muscle degeneration caused by gene mutations, the main symptoms are calf hypertrophy, hardness, difficulty in squatting, and landing on the soles of the feet before walking.

Muscular dystrophy refers to a group of inherited disorders characterized by progressively worsening muscle weakness and muscle degeneration that governs movement.

Muscular dystrophy is a muscle lesion caused by genetic mutations with progressive limb weakness as the main manifestation, and the common types are muscular dystrophy, including pseudohypertrophic muscular dystrophy, that is, gastrocnemius hypertrophy, which is more common in young boys; Facicoscapulohumeral muscular dystrophy, with facial muscle weakness, proximal upper limb weakness, and pterygoid scapula; and myotonic dystrophy, in which stiffness of the hands is the main manifestation, along with weakness of the hands and feet. Electromyography, genetic testing, and if necessary, muscle MRI and muscle pathology are usually done. Because of its insidious onset, it needs to be differentiated from myositis.

The most common type of muscular dystrophy is the DMD type in pseudohypertrophic muscular dystrophy, which is the most common X-linked recessive myopathy in China. Usually 3 to 5 years old insidious onset, prominent symptoms are pelvic girdle muscle weakness, manifested by slow walking, toe touching, easy falling. Difficulty ascending stairs and standing in a squatting position, typical duck steps may occur.

As symptoms worsen, Achilles tendon contractures, foot drop, and difficulty walking on flat ground may occur. The shoulder girdle muscles and upper arm muscles are often affected at the same time, but to a lesser extent, the two shoulder blades are erected on the back in a wing-like shape, called the winged scapula. Most children have muscle pseudohypertrophy that is tough to the touch, most notably the gastrocnemius muscle.

Patients may have comorbid myocardial damage, such as arrhythmias. By the age of 12, most children are unable to walk and need to use wheelchairs.

Muscular dystrophy, also known as progressive muscular dystrophy, is a group of genetic causes of muscle degeneration. The name "muscular dystrophy" is easy to mislead non-professionals, thinking that this group of diseases is related to nutrition, but in fact, the onset of muscular dystrophy has nothing to do with nutrition, and it cannot be achieved through nutritional supplementation. To establish a correct understanding of this group of diseases, let's take a look at its English name:

The key word here is dystrophy, we know that the root of the word dys- means bad, abnormal, and -trophy means hyperplasia, growth, so it refers to poor muscle growth

Muscular dystrophy is characterized by progressive muscle atrophy and weakness caused by various causes, as well as degeneration of the muscles that dominate movement. Generally, it is a congenital and hereditary disease, because of the abnormality or mutation of genes. The main manifestation is progressive atrophy and weakness of the muscles of the skeletal muscles, some of which can involve the heart muscle, that is, the muscles of the heart, and the clinical manifestations can be divided into several types:

Clause. 1. Pseudohypertrophic muscular dystrophy, a more serious pseudohypertrophic muscledystrophy, is mainly manifested as onset at the age of 2-8 years, clumsy walking, easy to fall, unable to run, climbing stairs, as well as spinal cord protrusion and lumbar bulge;

Clause. 2. Manifested as interfacial arch-shaped malnutrition, mainly the face can not show teeth, can not protrude lips, can not close eyes, can not frown, etc.;

Clause. 3. Manifested as malnutrition of the girdle muscles, which mainly affects the girdle muscles and psoas muscles of the pelvis, resulting in difficulty in walking, inability to climb stairs, swaying gait, frequent falls, etc.

This muscular dystrophy is a hereditary disease, which is more difficult, and Western medicine is generally through exercise and hormones. However, traditional Chinese medicine is carried out through the method of tonifying the kidney and producing sperm in the main bone through traditional Chinese medicine, and the general effect is not very good.

What is the cause of muscular dystrophy, the occurrence of muscular dystrophy is mainly related to genetic factors, when the patient's body has a large number of deletions and duplications of genes will lead to the occurrence of this disease, once the disease is serious, it will lead to paralysis of the patient, so the patient must pay attention to this disease.

Create a good environment, maintain reasonable expectations, and avoid overprotection. To maintain a comfortable mood and exercise appropriately, the patient's family should cooperate with the massage, and the patient himself should overcome difficulties and insist on proper exercise.