What can muscle atrophy be divided into? What are the signs of muscle atrophy?

Muscle atrophy is a relatively harmful disease in life, with a high incidence and serious harm to the health of patients. Disuse muscle atrophy: Disuse muscle atrophy is the most common type, usually caused by infection by other diseases, or long-term lack of labor.

Myogenic muscle atrophy: It is usually caused by nutritional disorders, ischemia, peripheral nerve lesions, etc., and the difficulty of this muscle atrophy is greater than that of disuse muscle atrophy, but it can still be done scientifically.

Neurogenic muscle atrophy: usually caused by lesions of the spine and lower motor neurons, the most serious and the most difficult, this type of muscle atrophy, often involving nerve roots, plexus and other neuronal lesions, is mostly genetic factors.

Muscle atrophy is divided into neurogenic muscle atrophy, myogenic muscle atrophy, and disuse muscle atrophy.

The so-called neurogenic muscular atrophy is muscle atrophy secondary to the nerve disorder that innervates the muscles, and the common one is Guillain-Barré peripheral neuropathy, and it is very likely that the muscle atrophy will be secondary to it in the late stage.

Myogenic muscle atrophy is caused by diseases of the muscles themselves, such as polymyositis, dermatomyositis, etc. Patients who do not use muscles for a long time, such as limb paralysis, may be complicated by disuse muscle atrophy. Patients with muscle atrophy may have improved movement disorders and reduced symptoms of paralysis by doing some regular ** at an early stage.

Disuse muscle atrophy may be caused by central paralysis and osteoarticular diseases, and once it is lifted, the patient can recover.

Which one exactly. Go to the hospital and ask the doctor to define it based on your physical condition, don't believe it too much, just use it as a reference.

It can be seen for a variety of reasons, mainly due to nervous system or muscle lesions, which need to be examined and diagnosed by electromyography and muscle biopsy, or it may be a symptom caused by nerve compression, such as cervical lumbar disc herniation, or it may be caused by central nervous disease, such as cerebral hemorrhage or cerebral infarction, which will manifest as sensory and motor disorders in the limbs.

Muscle atrophy from the outside**, that is, you can't see the lines of the muscles, giving people a feeling of shriveled and relaxed! Your body will feel less powerful and your balance will deteriorate!

Muscle atrophy is manifested by getting thinner and thinner. Becoming more and more uncomfortable.

Muscle wasting is a condition in which muscles become smaller due to muscle dystrophy. Intense long-term or repeated emotional changes such as nervousness, anxiety, irritability, and pessimism can cause the balance of excitatory and inhibitory processes in the cerebral cortex to be unbalanced, and make muscle beats aggravated.

What are the clinical manifestations of patients with muscle atrophy in Beijing Deshengmen Hospital of Traditional Chinese Medicine-Yin Shirong-Department of Impotence-Chief Physician-Muscular Dystrophy?

I feel it now, and my leg muscles are atrophiing.

It is obvious that the legs are not generally thick. One leg is thick and the other is thin.

Due to a herniated disc in the lumbar spine.

That's the characteristic!

In life, we must understand the symptoms of muscle atrophy, so that it can be detected and advanced in time at the early stage of the disease to prevent further aggravation of the disease.

1.Neurogenic amyotrophia: due to lower motor neurons and their damage.

When the anterior horn cells and brainstem motor nerve nuclei are damaged, the muscle atrophy is segmental, mostly distal to the limbs, symmetrical or asymmetrical, without sensory impairment, fasciculations often occur, and the degree of muscle strength and tendon reflexes is related to the degree of damage. Electromyography shows myofiber tremor potentials or high-amplitude motor unit potentials. Biopsy shows muscle atrophy and thinning.

Microscopic fascicular atrophy changes.

2.Myogenic atrophy: caused by a disease of the muscles themselves.

Atrophy is not distributed according to the nerve, usually proximal pelvic girdle and shoulder girdle symmetrical muscle atrophy, and rarely distal. With muscle weakness, no muscle fibrillation, and sensory deficits. Serum creatine phosphokinase, lactate dehydrogenase, aspartate aminotransferase, phosphoglucose mutase, and aldolase were all increased to varying degrees, and muscle weight phosphokinase was the most sensitive.

Electromyography is characterised by the presence of short-term multiphasic potentials.

3.Other: central amyotrophy is usually accompanied by hyperreflexia or pathological reflexes. Ischemic amyotrophy is mostly caused by various arteritis, thrombosis and other muscle ischemia and aseptic necrosis. Disuse amyotrophy is associated with long-term inactivity and is mostly reversible.

Muscle atrophy refers to the loss of striated muscle volume due to poor nutrition, thinning, or even loss of muscle fibers. The appearance of muscle tissue is mild, there is no protrusion, depression, relaxation, lack of muscle strength, and can resist exercise. Moderate depression with insufficient muscle strength and inability to do resistance exercises.

Severe associated bone exposure, severe muscle weakness, and lack of basic coordination.

Muscular atrophy is generally divided into disuse muscular atrophy, myogenic muscular atrophy, and neo-mesogenous muscular atrophy.