What are the symptoms of MND?

The main symptoms of motor neuron disease are muscle weakness and atrophy, but motor neuron disease is divided into many types according to the location of its onset, and there are several main types, we often say that there is amyotrophic sclerosis, this disease is often the distal end of the upper limbs, that is, the small muscles of the hands mainly begin to atrophy, and it is easy to fall off when holding things, and gradually develops to the opposite upper limbs, and then to the lower limbs; Another type is called bulbar palsy, its onset is the muscles of our throat or tongue muscles disease, then the main symptoms are the beginning of unclear speech, choking on drinking water, difficulty swallowing, this disease will progress relatively quickly, may soon develop to the upper limbs, the appearance of upper limb weakness; There are other types, such as primary lateral sclerosis, which often begins in the lower extremities, and it is more difficult to walk, and the disease progresses more slowly.

Patients with motor neurone disease mainly experience limb weakness and inflexibility. The first symptoms of motor neuron disease will start in the lower limbs, and then spread to the upper limbs, and the disease will worsen in the lower limbs, and the weakness of the limbs will be the main manifestations. Patients also have hyperreflexia and positive pathological reflexes.

In the later stages, the patient will have symptoms such as difficulty swallowing, slurred speech, and difficulty breathing. Therefore, once clinical symptoms appear, it is necessary to do it as soon as possible** to avoid dyspnea. Patients should also carry out appropriate exercises, which can also effectively prevent muscle atrophy.

Motor neuron disease (MND) is a chronic progressive neurodegenerative disease that selects the anterior horn cells of the spinal cord, motor neurons of the brainstem, pyramidal cells of the cortex, and pyramidal tract. Symptoms include upper and lower motor nervous system involvement, including muscle weakness, muscle atrophy, fasciculations and increased muscle tone, tendon hyperreflexia, and positive pathological signs. There is usually no paresthesia or urinary or bowel disorders.

Among them, muscle weakness, muscle atrophy, and fasciculations tremor are manifestations of lower motor nervous system involvement; Hypertonia, hyperreflexia, and positive pathological signs are the main manifestations of upper motor nervous system involvement.

The main clinical symptoms of motor neuron disease are as follows: 1. Movement disorders: including muscle atrophy, muscle beating and trembling, stiffness of hands and feet, inconvenience in walking, etc.; 2. Speech disorder:

Including dysarthria, tongue muscle atrophy, tongue muscle tremor, slurred speech, easy to choke, bulbar paralysis, etc.; 3. Pyramidal tract signs: including tendon hyperreflexia, positive pathological signs, increased muscle tone, etc.; 4. Normal autonomic nervous function: no sensory impairment, normal urine and bowel movements, and normal sexual function.

The early symptoms of motor neuron disease are mainly ineffective finger movement and weakness, followed by atrophy of small muscles of the hand, atrophy of the forearm and shoulder muscles, weakness of the lower limbs, difficulty walking, fasciculation, hyperreflexia, positive pyramidal tract signs, etc., any of the above manifestations should be treated in time for a clear diagnosis; Motor neuron disease** is mainly symptomatic**, and its common clinical manifestations are muscle weakness, muscle atrophy, increased muscle tone, positive pyramidal tract sign, fasciculations, etc.; It can be used symptomatic and supportive, such as supplementing vitamin E, B vitamins, etc.

Early symptoms are mild and can be easily confused with other diseases. Patients may only feel some symptoms such as weakness, flesh jumping, and fatigue easily, and gradually progress to generalized muscle atrophy and difficulty swallowing. Respiratory failure develops.

According to the clinical symptoms, it can be roughly divided into two types:

1.Limb-onset type.

Symptoms begin with progressive atrophy and weakness of the muscles in the limbs, and finally respiratory failure.

2.Bulbar onset.

Difficulty swallowing and speaking begins with early progression, and respiratory failure soon progresses.

Symptoms of motor neuron disease: fasciculations, muscular atrophy, muscle weakness, increased muscle tension, etc., ......Understand the symptoms of motor neuron disease for timely detection and treatment.

The clinical symptoms of motor neuron disease can be broadly divided into two types:

1.Limb onset: Symptoms are progressive atrophy and weakness of the muscles of the limbs, followed by respiratory failure.

2.Bulbar onset: Difficulty swallowing and speaking in the early stages, and respiratory failure soon progresses.

There are many symptoms of motor neuron disease, such as skewed walking, poor walking, and trembling.

Motor neuron diseases are a group of chronic progressive degenerative diseases that mainly damage the anterior horn of the spinal cord, the motor nucleus and pyramidal tract of the cranial nerve, and the most common symptoms are muscle atrophy and muscle weakness.

The exact form of MND is not too clear, and there is no specific method, so whether your condition is related to this still needs some corresponding examinations. The symptoms of recompulsion at this age are estimated to be related to gene deletion or underdevelopment, and genetic testing is recommended to rule out congenital diseases before proceeding**. Help is required to send all information (including MRI of the cerebrocervical and spinal cord**, electromyography), medical history, and medical records.

Tip**Improper paralysis can easily lead to paralysis.

The main display screen for MND is epilepsy, convulsions, etc.

There are many symptoms of motor neurons, such as the difficulty of using the hands, and the fact that some of them cannot speak in language.

This is needed. Professional doctors come to tell you that what most people tell you may not be very accurate, and I think what I can tell you is that the motor function is limited.

It is that you are prone to cramps when you exercise, and your legs, hands, and limbs are easily numb.

It's just not under your control. With more moxibustion, maybe it will be better.

Motor neurone disease, I think it reflects my avoidance of arrogance or emotional instability.

As for motor neurons, it includes that your body balance is relatively small, and then, other aspects are slower responses.

What are the symptoms of MND? You have to find an expert to answer this, you can check it on the Internet last time.

This situation is still relatively obvious, and it is recommended that we go to the hospital for a detailed examination before making a judgment.

Many times, many are not far away, and appreciation is key.

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Symptoms of motor neuron disease mainly include muscle weakness, muscle atrophy, bulbar palsy, pyramidal tract sign, etc. Muscle weakness and muscle atrophy: patients initially present with small muscle atrophy and weakness in one or both hands, which gradually develops to involve the forearm, upper arm and shoulder blades, and some patients begin to have muscle atrophy and weakness in the lower limbs, and eventually develop into generalized muscle atrophy and weakness after several or more years, and cannot take care of themselves.

What are the symptoms of motor neuron disease.

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The symptoms of the disease mainly include muscle weakness, muscle atrophy, bulbar paralysis, pyramidal tract signs, etc. Muscle weakness and muscle atrophy: patients initially present with small muscle atrophy and weakness in one or both hands, which gradually develops to involve the forearm, upper arm and shoulder blades, and some patients begin to have muscle atrophy and weakness in the lower limbs, and eventually develop into generalized muscle atrophy and weakness after several years or more than ten years, and cannot take care of themselves.

Hello dear, motor neurons are mainly some structures of the nervous system related to movement, anatomically it will be divided into upper motor nerve key meridian element and lower motor neuron, upper motor neuron refers to the brain center, some nerve cells on the cerebral cortex are called large pyramidal cells, and these cells will send out some nerve axons, these axons synapses form a nerve central nervous system, descending to the anterior horn cells of the spinal cord, to the part above the anterior horn cells of the spinal cord, all of which are called middle and upper motor neurons.

The clinical manifestations of motor neuron disease are mainly lack of strength and muscle atrophy, the muscle atrophy is mainly interosseous muscles and thenar muscles, no strength is first manifested as the inability to lift heavy objects, at this time the condition is mild, will not affect daily life, when the disease further develops, there may be dysphagia, hoarseness, etc., in severe cases, there will be paralysis of respiratory muscles, and then severe respiratory suffering and life-threatening, but the body's sensory nerves are not damaged, all sensations are normal.

Motor neuron is also known as ALS, as the name of the disease suggests, patients will gradually appear as if they are "frozen", and the patient will gradually develop from limb weakness to muscle atrophy; The limbs gradually develop from the hands and feet, and eventually to the torso. Patients may experience dyspnea, dysphagia, and most eventually die of paralysis of the respiratory muscles. At present, Western medicine does not have a good method for motor neurons, but there is no way for motor neurons, and choosing the right professional method as soon as possible plays a vital role in motor neurons.

Motor neuron is an incurable disease, and the most important thing is to treat the symptoms**, so that it will slowly recover.

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Manifested as limb weakness, tightness, and inactivity. Symptoms begin in both lower extremities and then spread to both upper extremities, with severe symptoms in the lower extremities. Weak limb strength, increased muscle tone, difficulty gait, spasmodic scissor gait, hyperreflexia, positive pathological reflexes.

If the lesion involves both cortical brainstems, symptoms of pseudobulbar palsy appear, manifesting as clear speech, dysphagia, and mandibular hyperreflexia.

The most common first symptom of amyotrophic lateral sclerosis is clumsiness and weakness in one or both fingers, followed by atrophy of the small finger muscles that progresses to the forearm, upper arm, and shoulder muscles. As the disease progresses, muscle weakness and atrophy extend to the trunk and neck, and eventually to the facial and laryngeal muscles. In a few cases, muscle atrophy and weakness begin in the lower extremities or trunk.

Fasciculations are often evident in the affected area. The common first symptom of progressive amyotrophy is atrophy and weakness of the small muscles in one or both hands, which gradually affects the muscles of the forearm, upper arm, and shoulder. Affected muscles are markedly atrophied, muscle tone is reduced, and muscle tremors may be seen.

Progressive bulbar palsy is characterized by progressive slurred articulation, dysphagia, choking on water, and weakness in chewing. The tongue muscles are obviously atrophied, and there are fasciculations, and the lip muscles and throat muscles are atrophied. This type of disease progresses rapidly, and most of them die within 1 to 2 years due to respiratory muscle paralysis or lung infection.

The common first symptom of primary lateral sclerosis is symmetrical stiffness and weakness in both lower extremities, with a scissor gait in walking. Progresses slowly and gradually affects both upper extremities. There is usually no muscle atrophy and fasciculations, and no sensory deficits.

This type progresses slowly and can survive for a long time. Other symptoms: A small percentage of patients with motor neuron disease have manifestations outside the motor system, such as dementia, paresthesias, and urinary and urinary dysfunction, and a small number of patients have extraocular muscle movement disorders.

Progressive muscle atrophy and analopathy paralysis are typical symptoms, and patients may have difficulty walking and daily activities, weakness of the lower limbs, slurred speech, and difficulty swallowing. It can be done through drugs** and traditional Chinese medicine**.

The early symptoms of motor neurons are not obvious, so many patients have difficulty wiping them in the early stage. The general course of the disease progresses slowly, but some types may progress more rapidly. Depending on the site of injury, the clinical manifestations are a different combination of muscle weakness, amyotrophy, and dysphagia.

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The early symptoms of MND are not obvious, so many patients in the early stages are difficult to detect. The general course of the disease progresses slowly, but some types may progress more rapidly. Depending on the site of injury, the clinical manifestations are a different combination of muscle weakness, muscle atrophy, and dysphagia.

Typical symptoms. Amyotrophic lateral sclerosis.

The first symptoms are clumsiness and weakness of one or both fingers, finger stiffness, followed by atrophy of the small muscles of the hand;

As the disease progresses, muscle atrophy extends to the forearms and lower limbs, and finally affects the face and throat, with significant fasciculations in the affected area;

In the advanced stage of the disease, weakness of tongue protrusion, difficulty swallowing, weakness in chewing, and slurred speech may occur;

In a few cases, muscle weakness and muscle atrophy may begin in the lower extremities;

Generally, there are no objective sensory disorders, but there are often subjective sensory disorders, such as numbness.

Progressive amyotrophy.

The first symptom is atrophy and stiffness of small muscles in one or both hands;

progressive involvement of the forearm, upper arm, and shoulder girdle muscles;

The affected muscles atrophy is obvious, muscle tone is reduced, fasciculations are visible, tendon reflexes are weakened, and pathological reflexes are reduced;

Sensory system and sphincter dysfunction are generally absent.

Progressive bulbar palsy.

slurred pronunciation, hoarseness, dysphagia, choking on water, weakness in chewing, and loss of gag reflex;

Sensory system and sphincter dysfunction are generally absent.

Primary lateral sclerosis.

The first symptoms are symmetrical stiffness and fatigue in both lower extremities, and walking with a scissor gait.

Progresses slowly and gradually affects the upper extremities.

Muscle tone in the extremities is increased, and muscle atrophy and fasciculations are generally absent.

The sensory system and sphincter are not affected.

Accompanying symptoms. Progressive bulbar palsy sometimes compromises both cortical brainstem tracts at the same time, resulting in forced crying and laughing and hypermandibular reflexes, resulting in the coexistence of true and pseudobulbar palsy.